MICRORUPTOR III SYST, Q-SWITCHED ND:YAG LASER COMP— 510(k) K895864

Name: FDA 510(k) clearance K895864
Creator: U.S. Food and Drug Administration
Published: 1989-12-29

Substantially Equivalent

Lasag AG

FDA 510(k) clearance K895864 for MICRORUPTOR III SYST, Q-SWITCHED ND:YAG LASER COMP, Substantially Equivalent on 1989-12-29. Applicant: Lasag AG. Device class: 2.

Clearance details

Applicant: Lasag AG
Product code: Code LXS
Device class: Class 2
Regulation: 21 CFR 886.4392
Advisory panel: Ophthalmic
Date received: 1989-10-03
Decision date: 1989-12-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Eden Prairie, MN, US

Download summary PDF View on FDA.gov ↗

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