Cruxi research & evidence
Biocompatibility Testing (ISO 10993 Program) evidence guides — page 18
Compare documented facts, dated analyses and evidence that can change your project scope. Confirm applicability with a specialist.
Compare Biocompatibility Testing (ISO 10993 Program) providers- Lascod Impression Materials (K201184): indications, design and recorded evidenceRegulatory decision evidence
- Laser Hair Growth Device (F21151, F21152, F21153, F21154, F21155, F21156, F21157, F21158, F21159) (K260899): indications, design and recorded evidenceRegulatory decision evidence
- Lenstec LC Injection system (K161776): indications, design and recorded evidenceRegulatory decision evidence
- Lianfa Safety Lancet (Five Models: NPA, PA, PA2, TPA, and APA) (K222376): indications, design and recorded evidenceRegulatory decision evidence
- Life Sensor Cardiac Monitor (K191331): indications, design and recorded evidenceRegulatory decision evidence
- Light Therapy System (M500, L6) (K251042): indications, design and recorded evidenceRegulatory decision evidence
- Lim Precision Steerable TS, Steerable Sheath, Dilator (K202226): indications, design and recorded evidenceRegulatory decision evidence
- LipiFlow Thermal Pulsation System (K161357): indications, design and recorded evidenceRegulatory decision evidence
- LithoVue Elite Single-Use Digital Flexible Ureteroscope - Standard (with pressure monitoring) (M0067940000); LithoVue Elite Single-Use Digital Flexible Ureteroscope - Reverse (with pressure monitoring) (M0067940500); LithoVue Elite Single-Use Digital Flexible Ureteroscope Standard (without pressure monitoring) (M0067941000); LithoVue Elite Single-Use Digital Flexible Ureteroscope Reverse (without pressure monitoring) (M0067941500) (K241598): indications, design and recorded evidenceRegulatory decision evidence
- Lollipop BiteBlock (K200652): indications, design and recorded evidenceRegulatory decision evidence
- Longeviti PorousFit implant (K211514): indications, design and recorded evidenceRegulatory decision evidence
- Luer Lock Syringe with Safety Needle; Luer Lock Syringe with Exchangeable Needle; Luer Lock Syringe with Blunt Fill Needle (K241821): indications, design and recorded evidenceRegulatory decision evidence
- Lumbar Expandable lnterbody Spacers -Additional Indications/Implants (K221894): indications, design and recorded evidenceRegulatory decision evidence
- Lumen 155-SF (K223911): indications, design and recorded evidenceRegulatory decision evidence
- Luminice (K214100): indications, design and recorded evidenceRegulatory decision evidence
- Lunderquist® Fixed Core Wire Guide (K181353): indications, design and recorded evidenceRegulatory decision evidence
- Lunoa System (K180608): indications, design and recorded evidenceRegulatory decision evidence
- M-Vizion Femoral Revision System Extension (K260173): indications, design and recorded evidenceRegulatory decision evidence
- M.U.S.T. Pedicle Screw System - Extension (K253940): indications, design and recorded evidenceRegulatory decision evidence
- MAASTRO Rectal Applicator Set (K252717): indications, design and recorded evidenceRegulatory decision evidence
- MADM (K140264): indications, design and recorded evidenceRegulatory decision evidence
- MAGEC Spinal Bracing and Distraction System (K233593): indications, design and recorded evidenceRegulatory decision evidence
- MALE CIRCUMCISION KITS:RAPIDECLAMP (K142163): indications, design and recorded evidenceRegulatory decision evidence
- MANDREL GUIDEWIRE (K140482): indications, design and recorded evidenceRegulatory decision evidence
- MARVEL Growing Rods (K213196): indications, design and recorded evidenceRegulatory decision evidence
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