Medical Device Manufacturer · US , Culver City , CA

Karl Storz Endoscopy - FDA 510(k) Cleared Devices

35 submissions · 35 cleared · Since 1995

35

Total

35

Cleared

0

Denied

FDA 510(k) Regulatory Record - Karl Storz Endoscopy General Hospital ✕

1 devices

1-1 of 1

Cleared Oct 25, 1996

KSEA MODEL 383320 20 ANGIOMAT

General Hospital · 266d