Applied Vascular Devices, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Applied Vascular Devices, Inc. - FDA 510(k) Cleared Devices
21
Total
21
Cleared
0
Denied
Applied Vascular Devices, Inc. has 21 FDA 510(k) cleared medical devices. Based in Santa Ana, US.
Historical record: 21 cleared submissions from 1988 to 1991. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Applied Vascular Devices, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Applied Vascular Devices, Inc.
21 devices
Cleared
Dec 23, 1991
SURGICAL OBTURATOR WITH SEAL
General & Plastic Surgery
250d
Cleared
Jul 05, 1991
DISPOSABLE SURGICAL TROCAR WITH SEAL
General & Plastic Surgery
87d
Cleared
May 29, 1991
AVD INTIMAX OCCLUSION CATHETER
Cardiovascular
121d
Cleared
Apr 26, 1991
INTIMAX THROMBECTOMY CATHETER
Cardiovascular
87d
Cleared
Apr 18, 1991
INTIMAX(TM) IRRIGATION CATHETER
Gastroenterology & Urology
31d
Cleared
Mar 28, 1991
AVD INTIMAX CHOLANGIOGRAPHY CATHETER
Gastroenterology & Urology
51d
Cleared
Mar 25, 1991
DIAGNOSTIC INTRASCULAR CATHETER
Cardiovascular
216d
Cleared
Mar 21, 1991
OPERATIVE CHOLANGIOGRAPHIC CATHETER
Gastroenterology & Urology
87d
Cleared
Feb 27, 1991
DISPOSABLE INTRODUCER SHEATH
General & Plastic Surgery
50d
Cleared
Feb 15, 1991
IRRIGATION CATHETER 4, 6 AND 10 FRENCH
Cardiovascular
270d
Cleared
Dec 21, 1990
SURGICAL TROCAR AND CANNULA
Obstetrics & Gynecology
87d
Cleared
Oct 19, 1990
ARTERIAL EMBOLECTOMY CATHETER
Cardiovascular
193d