Precision Laser Products, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Precision Laser Products, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Precision Laser Products, Inc. has 4 FDA 510(k) cleared medical devices. Based in Sellersville, US.
Historical record: 4 cleared submissions from 1991 to 1991. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Precision Laser Products, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Precision Laser Products, Inc.
4 devices
Cleared
Aug 20, 1991
PLP EVACUATION CONTROL SYSTEM 1 MICRO (ECS.1UM)
General Hospital
53d
Cleared
Jul 05, 1991
SINGLE-USE LAPAROSCOPIC SUCTION/IRRIGATION CANNULA
General & Plastic Surgery
121d
Cleared
Apr 08, 1991
PLP LAPAROSCOPIC CHOLECYSTECTOMY SET
General & Plastic Surgery
89d
Cleared
Feb 21, 1991
PLP LAPAROSCOPIC CHOLECYSTECTOMY DIS. ELEC. PROBES
General & Plastic Surgery
37d