Argus Medical Co., Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Argus Medical Co., Inc. has 6 FDA 510(k) cleared medical devices. Based in Walnut, US.
Historical record: 6 cleared submissions from 1995 to 1995.
Browse the FDA 510(k) cleared devices submitted by Argus Medical Co., Inc. Filter by specialty or product code using the sidebar.
6 devices
Cleared
Aug 24, 1995
ARGUS HYSTEROSCOPY INSTRUMENT SYSTEM
Obstetrics & Gynecology
213d
Cleared
Jul 26, 1995
ARGUS MEDICAL COMPANY LAPAROSCOPIC DISCECTOMY INSTRUMENT SYSTEM
Orthopedic
110d
Cleared
May 15, 1995
ARGUS ARTHROSCOPY INSTRUMENT SYSTEM
Orthopedic
115d
Cleared
Mar 03, 1995
ARGUS ENDOSCOPIC PLASTIC SURGERY INSTRUMENT SYSTEM
General & Plastic Surgery
37d
Cleared
Feb 17, 1995
ARGUS SINUS ENDOSCOPY INSTRUMENT SYSTEM
Ear, Nose, Throat
70d
Cleared
Feb 09, 1995
ARGUS LAPAROSCOPY INSTRUMENT SYSTEM
General & Plastic Surgery
9d