Medical Device Manufacturer · US , Elk Grove Village , IL

Kit Pak, Inc. - FDA 510(k) Cleared Devices

13 submissions · 4 cleared · Since 1989
13
Total
4
Cleared
0
Denied

Kit Pak, Inc. has 4 FDA 510(k) cleared medical devices. Based in Elk Grove Village, US.

Historical record: 4 cleared submissions from 1989 to 1995. Primary specialty: Gastroenterology & Urology.

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

FDA 510(k) Regulatory Record - Kit Pak, Inc.
13 devices
1-12 of 13
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