Medical Device Manufacturer · US , Vista , CA

Sensicon Corp. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1997

Total

Cleared

Denied

Sensicon Corp. has 2 FDA 510(k) cleared medical devices. Based in Vista, US.

Historical record: 2 cleared submissions from 1997 to 1998. Primary specialty: Obstetrics & Gynecology.

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

Sensicon Corp. 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 - Sensicon Corp.

2 devices

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