Cruxi research & evidence
FDA 510(k) Submission Services evidence guides — page 198
Compare documented facts, dated analyses and evidence that can change your project scope. Confirm applicability with a specialist.
Compare FDA 510(k) Submission Services providers- Tampon, Menstrual, Unscented (HEB) — FDA decisions, comparisons and evidenceFDA record research
- TandemLung Oxygenator (K153295): indications, design and recorded evidenceRegulatory decision evidence
- Tandry CMF Plate System (K220360): indications, design and recorded evidenceRegulatory decision evidence
- Tape And Bandage, Adhesive, Adjustable Closing Mechanism, Otc Use (PYO) — FDA decisions, comparisons and evidenceFDA record research
- Tapestry Biointegrative Implant (K212306): indications, design and recorded evidenceRegulatory decision evidence
- Tapestry Biointegrative Implant (K220867): indications, design and recorded evidenceRegulatory decision evidence
- Tapestry Biointegrative Implant (K252647): indications, design and recorded evidenceRegulatory decision evidence
- TauTona Pneumoperitoneum Assist Device (TPAD) (K233020): indications, design and recorded evidenceRegulatory decision evidence
- TeKBrace Knotless Anchor (K253538): indications, design and recorded evidenceRegulatory decision evidence
- Tear Pool Dissolvable Punctum Plugs (K190210): indications, design and recorded evidenceRegulatory decision evidence
- TechCare Trauma (K242171): indications, design and recorded evidenceRegulatory decision evidence
- Teco Creatinine Enzymatic Reagent Kit (K161527): indications, design and recorded evidenceRegulatory decision evidence
- TekBrace Solo Soft Tissue Reinforcement Device (K251063): indications, design and recorded evidenceRegulatory decision evidence
- Telemetry Monitor 5500 Release 4.0 (867232) (K242962): indications, design and recorded evidenceRegulatory decision evidence
- Telepack X LED (K182696): indications, design and recorded evidenceRegulatory decision evidence
- Tempo Tampon (K212277): indications, design and recorded evidenceRegulatory decision evidence
- Temporarily Implanted Peripheral Nerve Stimulation System For Sustained Pain Relief (SCN) — FDA decisions, comparisons and evidenceFDA record research
- Temporary Carotid Catheter For Embolic Capture (NTE) — FDA decisions, comparisons and evidenceFDA record research
- Tenderfoot (K223352): indications, design and recorded evidenceRegulatory decision evidence
- Tenex 2nd Generation System (K241700): indications, design and recorded evidenceRegulatory decision evidence
- TensCare KegelFit (K142506): indications, design and recorded evidenceRegulatory decision evidence
- Tera Harz Clear (K223355): indications, design and recorded evidenceRegulatory decision evidence
- Tera Lumbar Interbody Fusion System (Various PNs) (K251335): indications, design and recorded evidenceRegulatory decision evidence
- Test 5, 10-Methylenetetrahydrofolate Reductase Mutations, Genomic Dna Pcr (OMM) — FDA decisions, comparisons and evidenceFDA record research
- Test, Epithelial Ovarian Tumor Associated Antigen (He4) (OIU) — FDA decisions, comparisons and evidenceFDA record research
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