Laparomed Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Laparomed Corp. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Laparomed Corp. has 10 FDA 510(k) cleared medical devices. Based in Irvine, US.
Historical record: 10 cleared submissions from 1991 to 1994. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Laparomed Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Laparomed Corp.
10 devices
Cleared
Feb 25, 1994
FASCIA STITCHER
General & Plastic Surgery
158d
Cleared
Apr 20, 1993
LAPAROMED LAPAROSCOPIC RETRACTOR SYSTEM
General & Plastic Surgery
89d
Cleared
Aug 17, 1992
CATHETER CHOLANGIOGRAPHY
General & Plastic Surgery
116d
Cleared
Aug 06, 1992
LAPAROMED LIGATING LOOP
Ear, Nose, Throat
154d
Cleared
Jul 28, 1992
LAPAROSCOPIC RETRACTOR SYSTEM
Gastroenterology & Urology
147d
Cleared
Nov 07, 1991
ELECTROSURGICAL CUTTING/COAGULATION DEVICE/ACCESS
General & Plastic Surgery
57d
Cleared
Jul 02, 1991
LAPAROMED HOOK/SPATULA DEVICE
General & Plastic Surgery
175d
Cleared
Apr 08, 1991
LAPAROMED CHOLANGIOGRAM VACUUM DEVICE
General Hospital
81d
Cleared
Apr 08, 1991
LAPAROMED CHOLANGIOGRAM DEVICE
Gastroenterology & Urology
81d
Cleared
Mar 14, 1991
SUTURE APPLIER DEVICE
General & Plastic Surgery
84d