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. Cardiovascular ✕

5 devices

1-5 of 5

Cleared Aug 27, 1987

CORONARY ARTERY BYPASS GRAFT (CABG) MARKER

Cardiovascular · 161d

Cleared Dec 19, 1979

CASTROVIEJO VASCULAR SCISSORS

Cardiovascular · 6d

Cleared Oct 26, 1979

AORTIC OCCLUDER #000390

Cardiovascular · 9d

Cleared Sep 12, 1979

CARDIOVASCULAR INSTRUMENTS-VARIOUS

Cardiovascular · 16d

Cleared Mar 30, 1977

LOUISVILLE CLAMP PRODUCT #65-172

Cardiovascular · 14d