Medical Device Manufacturer · US , Mchenry , IL

Primrose Medical, Inc. - FDA 510(k) Cleared Devices

14 submissions · 14 cleared · Since 1984
14
Total
14
Cleared
0
Denied

Primrose Medical, Inc. has 14 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 14 cleared submissions from 1984 to 1989. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Primrose Medical, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Primrose Medical, Inc.

14 devices
1-14 of 14
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