K828583Substantially Equivalent

Lasermed Oculase Argon Laser

Name: K828583 Lasermed Oculase Argon Laser
Creator: Lasermed Corp.
Published: 1983-01-14
License: https://open.fda.gov/license/

Lasermed Corp., Costa Mesa CA / Traditional, Substantially Equivalent

FDA source

K828583 is the FDA 510(k) clearance record for LASERMED OCULASE ARGON LASER, cleared for Lasermed Corp. on 1983-01-14. FDA records list 7 510(k) clearances for Lasermed Corp., from 1983-01-14 to 1999-07-30. As of 2026-09-10, FDA records show no recalls naming K828583.

Clearance record

Decision date: 1983-01-14
Received: 1982-11-23 (52 days to decision)
Review panel: Unknown
Applicant: Lasermed Corp. 151 Kalmus Dr. Bldg. H-3, Costa Mesa CA
Third party review: No