Pfizer Laser Systems is one of 13679 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pfizer Laser Systems - FDA 510(k) Cleared Devices
Recent clearances: ORION YAG LASER SYSTEM OPHTHALMOLOGY, ORION, ORION YAG LASER SYSTEM EAR, NOSE, & THROAT APPLIC.
32
Total
32
Cleared
0
Denied
Pfizer Laser Systems has 32 FDA 510(k) cleared general & plastic surgery devices. Based in Irvine, US.
Historical record: 32 cleared submissions from 1988 to 1993.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pfizer Laser Systems
32 devices
Cleared
Nov 16, 1993
ORION YAG LASER SYSTEM OPHTHALMOLOGY
General & Plastic Surgery
998d
Cleared
Nov 16, 1993
ORION
General & Plastic Surgery
992d
Cleared
Feb 26, 1993
ORION YAG LASER SYSTEM EAR, NOSE, & THROAT APPLIC.
General & Plastic Surgery
744d
Cleared
Jun 16, 1992
POLARIS, GYNECOLOGY INDICATIONS
General & Plastic Surgery
403d
Cleared
Apr 15, 1992
ORION
General & Plastic Surgery
457d
Cleared
Dec 31, 1991
SIRIUS
General & Plastic Surgery
194d
Cleared
Nov 07, 1991
POLARIS, OPHTHALMOLOGY
General & Plastic Surgery
195d
Cleared
Oct 16, 1991
POLARIS, ORAL INDICATION
General & Plastic Surgery
160d
Cleared
Oct 11, 1991
POLARIS
General & Plastic Surgery
256d
Cleared
Oct 11, 1991
POLARIS, GASTROENTEROLOGY/UROLOGY/PULMONARY, GI/GU
General & Plastic Surgery
169d
Cleared
Jul 19, 1991
CENTAURI/PEGASUS
General & Plastic Surgery
203d
Cleared
Jul 11, 1991
CENTAURI YAG LASER SYST, GYNECOLOGY
General & Plastic Surgery
275d