Angiosystems, Inc. - FDA 510(k) Cleared Devices
14
Total
11
Cleared
0
Denied
Angiosystems, Inc. has 11 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 11 cleared submissions from 1984 to 1991. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Angiosystems, Inc. Filter by specialty or product code using the sidebar.
14 devices
Cleared
May 31, 1991
MEDICAL PROCEDURE KITS/ARTERIAL BLOOD SAMPLING
Anesthesiology
177d
Cleared
Apr 05, 1991
SURGICAL PROCEDURE TRAY/LAPAROSCOPY CHOLECYSTECTOM
General & Plastic Surgery
121d
Cleared
Mar 05, 1991
PROCEDURE KIT/ROUTINE DENTAL PROCEDURES
Dental
90d
Cleared
Feb 11, 1991
STERILE DISPOS SURGICAL DRAPE/C-SECTION DRAPE
General Hospital
68d
Cleared
Feb 11, 1991
STERILE DISPOSABLE SURGICAL DRAPE/ABDOMINAL DRAPE
General Hospital
68d
Cleared
Feb 06, 1991
STERILE DISPOSABLE DRAPE/OPHTHALMIC SURGERY
General Hospital
63d
Cleared
Feb 06, 1991
PROCEDURE TRAY/FOR VARIOUS OPHTHALMIC PROCEDURES
General & Plastic Surgery
63d
Cleared
Jan 22, 1991
GENERAL MEDICAL PROCEDURE KIT/SKIN PREPARATION
General Hospital
48d
Cleared
Jan 12, 1987
ARNOLD-KING PRESSURE DRESSING
General & Plastic Surgery
41d
Cleared
Sep 21, 1984
ANGIO SYS STERILE FIELD COVER
General & Plastic Surgery
32d
Cleared
Sep 21, 1984
ANGIO SYS BRACHIAL ANGIO DRAPE
General & Plastic Surgery
32d
Cleared
Sep 21, 1984
ANGIO SYS FLUOROSCOPE DRAPE
General & Plastic Surgery
32d
Cleared
Sep 21, 1984
ANGIOSYS FEMORAL ANGIOGRAPHY DRAPE
General Hospital
32d
Cleared
Sep 11, 1984
ANGIOSYSTEMS STANDARD ARTERIOGRAM & CARD
Cardiovascular
22d