Aomori Olympus Co., Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Aomori Olympus Co., Ltd. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Aomori Olympus Co., Ltd. has 7 FDA 510(k) cleared medical devices. Based in Melville, US.
Historical record: 7 cleared submissions from 2003 to 2005. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Aomori Olympus Co., Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Aomori Olympus Co., Ltd.
7 devices
Cleared
Jan 25, 2005
SONOSURG TROCAR
General & Plastic Surgery
168d
Cleared
Sep 08, 2004
SONOSURG ULTRASONIC SURGICAL SYSTEM
General & Plastic Surgery
90d
Cleared
Nov 14, 2003
SINGLE USE 3-LUMEN BALLOON CATHETER, MODELS B-230Q-A AND B-230Q-B
Gastroenterology & Urology
29d
Cleared
Oct 01, 2003
OLYMPUS ULTRASONIC SURGICAL SYSTEM
General & Plastic Surgery
139d
Cleared
Aug 29, 2003
OLYMPUS ULTRASONIC SURGICAL SYSTEM
General & Plastic Surgery
88d
Cleared
Apr 16, 2003
PANCREATIC DRAINAGE TUBE
Gastroenterology & Urology
330d
Cleared
Mar 28, 2003
MUCUS COLLECTION PROBE, MODELS BC-401C & BC-402C
Ear, Nose, Throat
246d