Circon Acmi - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Circon Acmi has 10 FDA 510(k) cleared medical devices. Based in Stamford, US.
Historical record: 10 cleared submissions from 1988 to 2002. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Circon Acmi Filter by specialty or product code using the sidebar.
10 devices
Cleared
Jan 18, 2002
USA SERIES LAPAROSCOPES
General & Plastic Surgery
119d
Cleared
Nov 17, 1998
AEH-3 ELECTROHYDRAULIC LITHOTRIPTER AND PROBES (E-1F, E-3F, E-5F, AND E-9F)
Gastroenterology & Urology
281d
Cleared
Feb 28, 1991
LAP 3501 HIGH FLOW INSUFFLATOR
Obstetrics & Gynecology
66d
Cleared
Feb 28, 1991
GYN-1500 HYSTEROSCOPIC INUFFLATOR
Obstetrics & Gynecology
66d
Cleared
Apr 17, 1989
MORRIS ANTI-SPLATTER DEVICE FOR ENDOSCOPES
Gastroenterology & Urology
201d
Cleared
Mar 03, 1989
CIRCON ACMI BICAP II THERAPEUTIC SYSTEM BC-200
Gastroenterology & Urology
162d
Cleared
Jan 11, 1989
CIRCON ACMI BICAP III THERAPEUTIC SYSTEM
Gastroenterology & Urology
92d
Cleared
Jan 10, 1989
CIRCON ACMI BICAP HEMORRHOID SYSTEM BH-10 & BHP-20
Gastroenterology & Urology
91d
Cleared
Jan 05, 1989
BICAP ABLATING FORCEPS BAF-7
Gastroenterology & Urology
84d
Cleared
Oct 17, 1988
BULLARD INTUBATING LARYNGOSCOPE LAR-A & LAR-P
Anesthesiology
39d