Advanced Surgical Intervention, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Advanced Surgical Intervention, Inc. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Advanced Surgical Intervention, Inc. has 9 FDA 510(k) cleared medical devices. Based in San Clemente, US.
Historical record: 9 cleared submissions from 1988 to 1996. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Advanced Surgical Intervention, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Advanced Surgical Intervention, Inc.
9 devices
Cleared
May 08, 1996
MINIGUARD
Gastroenterology & Urology
243d
Cleared
Jul 08, 1993
ASI LIGASURE(TM) SUTURE LIGATION INSTRUMENT
General & Plastic Surgery
217d
Cleared
Apr 29, 1993
ASI CYSTOLASE LASER CYSTOSCOPE
General & Plastic Surgery
93d
Cleared
Oct 28, 1992
ASI UROPLASTY LASER CYSTOSCOPE
General & Plastic Surgery
183d
Cleared
Aug 27, 1990
UROPLASTY TCU PROSTATIC URETHROPLASTY CATHETER
Gastroenterology & Urology
76d
Cleared
Jun 20, 1990
ASI HEMOSTASIS CATHETER
Gastroenterology & Urology
90d
Cleared
May 24, 1990
ASI TCU PROSTATIC URETHROPLASTY CATHETER & ACCESS.
Gastroenterology & Urology
176d
Cleared
Oct 24, 1989
ASI CYSTOSCOPE SHEATH, GRASPING FORCEPS & FOR.BODY
Gastroenterology & Urology
74d
Cleared
Jan 27, 1988
URETHRAL DILATOR ENDOSCOPE
Gastroenterology & Urology
85d