Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K904628Substantially Equivalent

Centauri Yag Laser Syst, Gastroenterology

Pfizer Laser Systems, Irvine CA / Traditional, Substantially Equivalent

K904628 is the FDA 510(k) clearance record for CENTAURI YAG LASER SYST, GASTROENTEROLOGY, a class II device, cleared for Pfizer Laser Systems on under FDA product code GEX (Powered Laser Surgical Instrument). FDA's definition for product code GEX reads: "A laser (light amplification by stimulated emission of radiation) based device having coherence, collimated and typically monochromatic radiation. Typically indicated to to cut, destroy, remove or coagulate tissue, generally soft tissue...". FDA records list 32 510(k) clearances for Pfizer Laser Systems, from to . As of , FDA records show no recalls naming K904628.

Clearance record

Decision date
Received
(90 days to decision)
Product code
GEX Powered Laser Surgical Instrument
Regulation
21 CFR 878.4810
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Pfizer Laser Systems 3 Morgan, Irvine CA
Third party review
No

Clearances, product code GEX

Trailing 12 months
68 clearances under product code GEX in the twelve months to October 2026, November 2025 the highest month at 11.
Show the numbers
Monthly 510(k) clearances under FDA product code GEX, trailing twelve months
MonthClearances
November 202511
December 20255
January 20264
February 20266
March 20267
April 20265
May 20268
June 20263
July 20264
August 20264
September 202611
October 20260