Medical Device Manufacturer · US , Hunt Valley , MD

Precision Endoscopy of America, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1997

Total

Cleared

Denied

Precision Endoscopy of America, Inc. has 1 FDA 510(k) cleared medical devices. Based in Hunt Valley, US.

Historical record: 1 cleared submissions from 1997 to 1997. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Precision Endoscopy of America, Inc. Filter by specialty or product code using the sidebar.

Precision Endoscopy of America, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Precision Endoscopy of America, Inc.

1 devices

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