Cruxi research & evidence
Biocompatibility Testing (ISO 10993 Program) evidence guides — page 17
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- Juell 3D Volo Base (K181220): indications, design and recorded evidenceRegulatory decision evidence
- KANGAROO ENTERAL FEEDING SET WITH ENFIT CONNECTORS (K141479): indications, design and recorded evidenceRegulatory decision evidence
- KATANA Zirconia ONE For IMPLANT (K233285): indications, design and recorded evidenceRegulatory decision evidence
- KHEIRON® Spinal Fixation System, including patient specific K-ROD (K253802): indications, design and recorded evidenceRegulatory decision evidence
- KIRO Set (K152441): indications, design and recorded evidenceRegulatory decision evidence
- KITAZATO IUI CATHETER (K131491): indications, design and recorded evidenceRegulatory decision evidence
- KOGENT SPETZLER LIGHTED SUCTION TUBES (K141781): indications, design and recorded evidenceRegulatory decision evidence
- KP Protective Face Mask (K243342): indications, design and recorded evidenceRegulatory decision evidence
- KYOLING CPR Mask with Oxygen Port and Without Oxygen Port (K142764): indications, design and recorded evidenceRegulatory decision evidence
- KardiFlex NC Coronary Dilatation Catheter (K202578): indications, design and recorded evidenceRegulatory decision evidence
- LAITEST Medical Face Mask (K214035): indications, design and recorded evidenceRegulatory decision evidence
- LATERA Absorbable Nasal Implant System (K192661): indications, design and recorded evidenceRegulatory decision evidence
- LED Light Therapy Device (KFB290, KFB291, KFB265, KFB293) (K241857): indications, design and recorded evidenceRegulatory decision evidence
- LED Light Therapy Device (Models: SG-FM, SG-FE) (K253086): indications, design and recorded evidenceRegulatory decision evidence
- LIFEPAK® 35 AC Power Adapter (41335-000001) (K240162): indications, design and recorded evidenceRegulatory decision evidence
- LIFEPAK® Invasive Pressure Adapter Cable (Interfaces with ICU Medical Transpack IV Invasive Pressure Transducers (or equivalent)) (11230-000021); LIFEPAK® Invasive Pressure Adapter Cable (interfaces with Edwards Lifesciences TruWave Invasive Pressure Transducers (or equivalent)) (11230-000024) (K240156): indications, design and recorded evidenceRegulatory decision evidence
- LIGACLIP 12mm L Endoscopic Rotating Multiple Clip Applier (K181488): indications, design and recorded evidenceRegulatory decision evidence
- LIXI (LXOSFM1) (K253662): indications, design and recorded evidenceRegulatory decision evidence
- LOGIQ E10s (K251963): indications, design and recorded evidenceRegulatory decision evidence
- LOGIQ Focus (K261835): indications, design and recorded evidenceRegulatory decision evidence
- LTM-Perforated Surgical Mesh (K150712): indications, design and recorded evidenceRegulatory decision evidence
- Laminar P1 (LDH-HW-001) (K242487): indications, design and recorded evidenceRegulatory decision evidence
- Lancet (I, II, III, V, VI); Lancing device (HH-X-T, HH-XIII-T, HH-XV-T, HH-XVI-T, HH-XVII-T, HH-XVIII-T, HH-XIX, HH-XXI-T, HH-XXII-T, HH-XXIII-T, HH-XXIV-T) (K220475): indications, design and recorded evidenceRegulatory decision evidence
- LaparoLight Veress Needle (K171139): indications, design and recorded evidenceRegulatory decision evidence
- Lapidus Screw Kit (K262075): indications, design and recorded evidenceRegulatory decision evidence
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