Karl Storz Endoskop GmbH - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Karl Storz Endoskop GmbH has 11 FDA 510(k) cleared medical devices. Based in Culver City, US.
Historical record: 11 cleared submissions from 1994 to 1997.
Browse the FDA 510(k) cleared devices submitted by Karl Storz Endoskop GmbH Filter by specialty or product code using the sidebar.
11 devices
Cleared
Nov 07, 1997
KSEA INSTRUMENT SET FOR SAPHENOUS VEIN HARVESTING
General & Plastic Surgery
81d
Cleared
Aug 29, 1996
KSEA VAPORIZATION ELECTRODES
Gastroenterology & Urology
119d
Cleared
Sep 18, 1995
LUER, JACKSON TRACHEA TUBES, LUER SPEAKING TRACHEA TUBES
Anesthesiology
62d
Cleared
Jun 30, 1995
TORCARS,CANNULAE,SHEATHS,OBTURATORS
Obstetrics & Gynecology
333d
Cleared
May 24, 1995
KARL STORZ CATHETERS, MANDRIN, PLUGS, CONNECTOR
Gastroenterology & Urology
26d
Cleared
Mar 21, 1995
KSEA SEMM TISSUR PUNCH
Obstetrics & Gynecology
267d
Cleared
Nov 07, 1994
CHOLANGIOGRAPHY SET
General & Plastic Surgery
112d
Cleared
Nov 02, 1994
KARL STORZ INSULATED DISSECTING CANNULAE, CANNULAE, SUCTION TUBES, INSERT TUBES
General & Plastic Surgery
34d
Cleared
Oct 14, 1994
RIGID TELESCOPES
Ear, Nose, Throat
64d
Cleared
Sep 14, 1994
TROCARS,CANNULAE,SHEATHS,OBTURATORS
Gastroenterology & Urology
47d
Cleared
Aug 24, 1994
TROCARS,CANNULAE, SHEATHS
Ear, Nose, Throat
19d