Cruxi research & evidence
FDA 510(k) Submission Services evidence guides — page 77
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- FIAGON NAVIGATION SYSTEM (K133573): indications, design and recorded evidenceRegulatory decision evidence
- FIBERION OPHTHALMIC ENDOLASER PROBE (K133019): indications, design and recorded evidenceRegulatory decision evidence
- FILASILK - Natural Non-absorbable Silk Surgical Suture, FILAMIDE - Non Absorbable polyamide surgical Sutures, MERICRON XL - Non Absorbable Polyester Surgical Suture, FILAPROP - Non Absorbable Polypropylene surgical Suture (K160623): indications, design and recorded evidenceRegulatory decision evidence
- FILTRAY 2G Disposable Water Filters (K191563): indications, design and recorded evidenceRegulatory decision evidence
- FIRST CVSS v4.0 — FDA recognition transition and report handoffCompliance research
- FIX-C 3D Ti ACIF System (K243915): indications, design and recorded evidenceRegulatory decision evidence
- FIXIT Threaded Anchor System (K170868): indications, design and recorded evidenceRegulatory decision evidence
- FLAMENCO SPINAL FIXATION SYSTEM (K102853): indications, design and recorded evidenceRegulatory decision evidence
- FLEX Monoclonal Mouse Anti-Human Progesterone Receptor, Clone PgR 1294, Ready-to-Use (Dako Omnis) (K170005): indications, design and recorded evidenceRegulatory decision evidence
- FLEX Monoclonal Rabbit Anti-Human Estrogen Receptor a, Clone EPI, RTU (Dako Onmis) (K170028): indications, design and recorded evidenceRegulatory decision evidence
- FLEX Vessel Prep System (K202187): indications, design and recorded evidenceRegulatory decision evidence
- FLEXIBLE VIDEO-URETERO-RENOSCOPE SYSTEM (K141250): indications, design and recorded evidenceRegulatory decision evidence
- FLEXICARE FL-9000U RESPIRATORY HUMIDIFIER BASE (K161314): indications, design and recorded evidenceRegulatory decision evidence
- FLEXICARE NEONATAL HEATED WIRE BREATHING SYSTEM (K160540): indications, design and recorded evidenceRegulatory decision evidence
- FLOWRUNNER Aspiration System (K251488): indications, design and recorded evidenceRegulatory decision evidence
- FLOWRUNNER Aspiration System (K254208): indications, design and recorded evidenceRegulatory decision evidence
- FLUOBEAM 800 CLINIC LASER IMAGING DEVICE AND FLUOCASE 800 CONTROL SYSTEM (K132475): indications, design and recorded evidenceRegulatory decision evidence
- FLUOBEAM® LX Imaging System (FB-LX); FLUOBEAM® LX Red Imaging System (FB-LXR) (K233564): indications, design and recorded evidenceRegulatory decision evidence
- FLUOBEAM® LX Red (K230898): indications, design and recorded evidenceRegulatory decision evidence
- FM-3000 FETAL MONITOR (K141194): indications, design and recorded evidenceRegulatory decision evidence
- FONA XDC (K222274): indications, design and recorded evidenceRegulatory decision evidence
- FORA G90 PERFORM BLOOD GLUCOSE MONITORING SYSTEM (K100405): indications, design and recorded evidenceRegulatory decision evidence
- FORA GTel Blood Glucose Monitoring System (K173505): indications, design and recorded evidenceRegulatory decision evidence
- FORA V20 BLOOD GLUCOSE MONITORING SYSTEM (K100406): indications, design and recorded evidenceRegulatory decision evidence
- FORMA Composite (Shade A3D) (K240694): indications, design and recorded evidenceRegulatory decision evidence
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