Asap Endoscopic Products GmbH is one of 481 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Asap Endoscopic Products GmbH - FDA 510(k) Cleared Devices
Recent clearances: ASAP MUITISCOPE, ASAP SINUSCOPE 10-0036-00,10-0037-00,10-0038,10-0039-00,10-0040-00,10-0041-00,10-0042-00,10-0043-00,10-0044-00,10-0045-0, ASAP HYSTEROSCOPE AND GYNECOLOGIC LAPAROSCOPE (SURGERY) 10-00018-00, 10-0019-00, 100020-00, 10-0021-00, 10-0022-00, 10-0
5
Total
5
Cleared
0
Denied
Asap Endoscopic Products GmbH has 5 FDA 510(k) cleared medical devices. Based in Luebeck, DE.
Historical record: 5 cleared submissions from 2003 to 2013. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Asap Endoscopic Products GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Asap Endoscopic Products GmbH
5 devices
Cleared
Jan 08, 2013
ASAP MUITISCOPE
Orthopedic
257d
Cleared
Jan 08, 2004
ASAP SINUSCOPE...
Ear, Nose, Throat
120d
Cleared
Sep 29, 2003
ASAP HYSTEROSCOPE AND GYNECOLOGIC LAPAROSCOPE (SURGERY) 10-00018-00,...
Obstetrics & Gynecology
95d
Cleared
Sep 15, 2003
ASAP ARTHROSCOPE MODELS
Orthopedic
81d
Cleared
Jun 30, 2003
ASAP CYSTOSCOPE
Gastroenterology & Urology
81d