Medical Device Manufacturer · US , Fort Myers , FL

Sims - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1997

Total

Cleared

Denied

Sims has 2 FDA 510(k) cleared medical devices. Based in Fort Myers, US.

Historical record: 2 cleared submissions from 1997 to 1997. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Sims Filter by specialty or product code using the sidebar.

Sims is one of 12845 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Sims

2 devices

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