Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K837235Substantially Equivalent

Model 920 Argon Laser System

Coherent Radiation Laboratories, Walker MI / Traditional, Substantially Equivalent

K837235 is the FDA 510(k) clearance record for MODEL 920 ARGON LASER SYSTEM, cleared for Coherent Radiation Laboratories on . FDA records list 3 510(k) clearances for Coherent Radiation Laboratories, from to . As of , FDA records show no recalls naming K837235.

Clearance record

Decision date
Received
(34 days to decision)
Review panel
Unknown
Applicant
Coherent Radiation Laboratories 4221 Richmond Rd., NW, Walker MI
Third party review
No