Akcess Medical Products, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Akcess Medical Products, Inc. - FDA 510(k) Cleared Devices
36
Total
28
Cleared
0
Denied
Akcess Medical Products, Inc. has 28 FDA 510(k) cleared gastroenterology & urology devices. Based in New Brunswick, US.
Historical record: 28 cleared submissions from 1989 to 1994.
Browse the complete list of FDA 510(k) cleared gastroenterology & urology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Akcess Medical Products, Inc.
36 devices
Cleared
Oct 07, 1994
SILICONE CATHETER REPAIR KITS
Gastroenterology & Urology
654d
Cleared
Aug 02, 1994
AKCESS0CATH KIT
Gastroenterology & Urology
623d
Cleared
Apr 05, 1994
AKCESS-CATH
Gastroenterology & Urology
504d
Cleared
Feb 07, 1994
RIGHT ATRIAL CATHETER
General Hospital
364d
Cleared
Jan 14, 1994
SPLITTABLE SHEATH INTRODUCER SET
Gastroenterology & Urology
702d
Cleared
Jan 14, 1994
COAXIAL ACUTE CATHETER
Gastroenterology & Urology
316d
Cleared
Apr 23, 1992
CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATH SET
Gastroenterology & Urology
171d
Cleared
Apr 22, 1992
RIGHT ATRIAL CATHETER KITS
Cardiovascular
90d
Cleared
Apr 10, 1992
AKCESS-CATH KIT
Gastroenterology & Urology
168d
Cleared
Mar 27, 1992
CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATH. KITS
Gastroenterology & Urology
130d
Cleared
Sep 23, 1991
RIGHT ATRIAL CATHETERS
Cardiovascular
181d
Cleared
Apr 29, 1991
PERMANENT SILICONE CATHETERS
Gastroenterology & Urology
83d