LASERSCOPE OMNI PLUS PHOTOSURGICAL SYSTEM/SUPPLEM— 510(k) K862598

Name: FDA 510(k) clearance K862598
Creator: U.S. Food and Drug Administration
Published: 1986-11-19

Substantially Equivalent

Laserscope

FDA 510(k) clearance K862598 for LASERSCOPE OMNI PLUS PHOTOSURGICAL SYSTEM/SUPPLEM, Substantially Equivalent on 1986-11-19. Applicant: Laserscope. Device class: 2.

Clearance details

Applicant: Laserscope
Product code: Code LNK
Device class: Class 2
Regulation: 21 CFR 878.4810
Advisory panel: General, Plastic Surgery
Date received: 1986-07-01
Decision date: 1986-11-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Santa Clara, CA, US

Download summary PDF View on FDA.gov ↗

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