Medical Device Manufacturer · US , Mchenry , IL

Edward Weck, Inc. - FDA 510(k) Cleared Devices

140 submissions · 140 cleared · Since 1976

Recent clearances: WECK TROCAR, LM15(TM), CATALOG NUMBER - 523821, HEMOCLIP II

140
Total
140
Cleared
0
Denied

FDA 510(k) Regulatory Record - Edward Weck, Inc. Ear, Nose, Throat

17 devices
1-17 of 17
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