Medical Device Manufacturer · US , Mchenry , IL

Corpak Co. - FDA 510(k) Cleared Devices

21 submissions · 20 cleared · Since 1981
21
Total
20
Cleared
0
Denied

Corpak Co. has 20 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 20 cleared submissions from 1981 to 1996. Primary specialty: Gastroenterology & Urology.

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

FDA 510(k) Regulatory Record - Corpak Co.

21 devices
1-12 of 21
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