National Advanced Endoscopy Devices, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
National Advanced Endoscopy Devices, Inc. has 8 FDA 510(k) cleared medical devices. Based in Canoga Park, US.
Historical record: 8 cleared submissions from 1999 to 2017.
Browse the FDA 510(k) cleared devices submitted by National Advanced Endoscopy Devices, Inc. Filter by specialty or product code using the sidebar.
8 devices
Cleared
Aug 01, 2017
AED Sinuscope
Ear, Nose, Throat
183d
Cleared
Jan 07, 2015
AED HYSTEROSCOPE AND ACCESSORIES
Obstetrics & Gynecology
212d
Cleared
Dec 30, 2010
AED RESECTOSCOPE
Gastroenterology & Urology
106d
Cleared
Sep 29, 2008
AED BIPOLAR FORCEPS, MODEL 13-1646
General & Plastic Surgery
118d
Cleared
Sep 25, 2008
AED MONOPOLAR LAP ACCESSORIES
General & Plastic Surgery
119d
Cleared
Dec 15, 1999
AED CYSTOSCOPE
Gastroenterology & Urology
44d
Cleared
Dec 06, 1999
AED LAPAROSCOPE
General & Plastic Surgery
35d
Cleared
Dec 02, 1999
AED ARTHROSCOPE
Orthopedic
203d