LASER PHOTOCOAGULATOR ARGON MED. LASER— 510(k) K813429

Name: FDA 510(k) clearance K813429
Creator: U.S. Food and Drug Administration
Published: 1982-01-22

Substantially Equivalent

American Laser Corp.

FDA 510(k) clearance K813429 for LASER PHOTOCOAGULATOR ARGON MED. LASER, Substantially Equivalent on 1982-01-22. Applicant: American Laser Corp.. Device class: 2.

Clearance details

Applicant: American Laser Corp.
Product code: Code HPJ
Device class: Class 2
Regulation: 21 CFR 886.1360
Advisory panel: Ophthalmic
Date received: 1981-12-08
Decision date: 1982-01-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.