Medical Device Manufacturer · US , Mchenry , IL

Zimmar Consulting , Ltd. - FDA 510(k) Cleared Devices

17 submissions · 17 cleared · Since 1984
17
Total
17
Cleared
0
Denied

Zimmar Consulting , Ltd. has 17 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 17 cleared submissions from 1984 to 1986. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Zimmar Consulting , Ltd. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Zimmar Consulting , Ltd.

17 devices
1-12 of 17
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