Cruxi research & evidence
FDA 510(k) Submission Services evidence guides — page 189
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- Sterile Aesthetic Cannula and Hypodermic Needle (K223327): indications, design and recorded evidenceRegulatory decision evidence
- Sterile Auto-Disable Syringes with/without Needle for Single Use (K231727): indications, design and recorded evidenceRegulatory decision evidence
- Sterile Disposable Syringes (K172694): indications, design and recorded evidenceRegulatory decision evidence
- Sterile Hypodermic Syringe for Single Use (20ml, 30ml, 50ml, 60ml) (K252279): indications, design and recorded evidenceRegulatory decision evidence
- Sterile Hypodermic Syringe for Single Use, with/without Needle, Sterile Hypodermic Needle for Single Use (K212846): indications, design and recorded evidenceRegulatory decision evidence
- Sterile Hypodermic Syringes for Single Use (K213811): indications, design and recorded evidenceRegulatory decision evidence
- Sterile Insulated Dilators, 5, 10, 16mm (MDT-0442S); Sterile, Insulated Dilator, 20mm (MDT-0469S) (K253580): indications, design and recorded evidenceRegulatory decision evidence
- Sterile Syringe with Fixed Safety Needle for Single Use (K212652): indications, design and recorded evidenceRegulatory decision evidence
- Sterile Water for Inhalation in 1L Flexoval ® bottles. (K223551): indications, design and recorded evidenceRegulatory decision evidence
- Sterile and Non-Sterile Ultrasound Gels (K232957): indications, design and recorded evidenceRegulatory decision evidence
- Sterile syringes for single use with/without needle (K231729): indications, design and recorded evidenceRegulatory decision evidence
- Sterilizer Automated Loading System (PEC) — FDA decisions, comparisons and evidenceFDA record research
- Steripath Gen2 Blood Collection System (K192247): indications, design and recorded evidenceRegulatory decision evidence
- Sterisheet Sterilization Wrap (K152291): indications, design and recorded evidenceRegulatory decision evidence
- Steth IO Spot (K220196): indications, design and recorded evidenceRegulatory decision evidence
- Stethophone Pro (K252595): indications, design and recorded evidenceRegulatory decision evidence
- StimOnTM Pain Relief System (GM2439) (K213802): indications, design and recorded evidenceRegulatory decision evidence
- StimSite (K200886): indications, design and recorded evidenceRegulatory decision evidence
- Stimulator Kit, Trial Kit, Spare Lead Kit, Wearable Assembly Kit (K180981): indications, design and recorded evidenceRegulatory decision evidence
- Stimulator, Electrical, Transcutaneous, For Arthritis (NYN) — FDA decisions, comparisons and evidenceFDA record research
- Stimulator, Intramuscular, Automatic (NRW) — FDA decisions, comparisons and evidenceFDA record research
- Stimulator, Muscle, Powered, For Muscle Conditioning (NGX) — FDA decisions, comparisons and evidenceFDA record research
- Stimulator, Nerve, Electrical, Percutaneous (Pens), For Pain Relief (NHI) — FDA decisions, comparisons and evidenceFDA record research
- Stimulator, Nerve, Electrical, Transcutaneous, Limited Output, Arthritis Pain Relief (OCF) — FDA decisions, comparisons and evidenceFDA record research
- Stimulator, Nerve, Transcutaneous, Over-The-Counter (NUH) — FDA decisions, comparisons and evidenceFDA record research
Page 189 of 228