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.
FDA 510(k) cleared devices by Angiosystems, Inc.
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