Access Surgical Intl., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Access Surgical Intl., Inc. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Access Surgical Intl., Inc. has 9 FDA 510(k) cleared medical devices. Based in Bedminster, US.
Historical record: 9 cleared submissions from 1992 to 1995. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Access Surgical Intl., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Access Surgical Intl., Inc.
9 devices
Cleared
Nov 29, 1995
BLADE, SCALPEL & BLADE, HANDEL
Gastroenterology & Urology
61d
Cleared
Sep 12, 1995
ACCESS POINT
General & Plastic Surgery
56d
Cleared
Jan 12, 1995
ACCESS SURGICAL INT'L THORACIC ENDOSCOPIC SURGICAL INSTRUMENTS
General & Plastic Surgery
59d
Cleared
Nov 08, 1994
ACCESS POINT
General & Plastic Surgery
28d
Cleared
Mar 29, 1994
FLEX-I-PORT
General & Plastic Surgery
49d
Cleared
Nov 18, 1993
ACCESS SURGICAL INT'L INC. ENDOSCOPIC SURG. INST.
General & Plastic Surgery
141d
Cleared
Nov 25, 1992
ACCESS SURGICAL INT'L ENDOSCOPIC SURGICAL INSTRUM.
General & Plastic Surgery
188d
Cleared
Nov 18, 1992
ACCESS SURGICAL BIPOLAR ENDOSCOPIC SURG. INSTRUM.
General & Plastic Surgery
181d
Cleared
Nov 17, 1992
ACCESS SURGICAL MONOPOLAR ENDOSCOPIC SURG. INSTRUM
General & Plastic Surgery
180d