Medical Device Manufacturer · US , Lenexa , KS

Entracare Corp. - FDA 510(k) Cleared Devices

3 submissions · 2 cleared · Since 1994

Total

Cleared

Denied

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

Historical record: 2 cleared submissions from 1994 to 1997. Primary specialty: General Hospital.

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

Entracare 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 - Entracare Corp.

3 devices

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