LASERMATIC SURGILASER MODEL 5050— 510(k) K870587

Name: FDA 510(k) clearance K870587
Creator: U.S. Food and Drug Administration
Published: 1988-08-10

Substantially Equivalent for Some Indications

Lasermatic OY

FDA 510(k) clearance K870587 for LASERMATIC SURGILASER MODEL 5050, Substantially Equivalent for Some Indications on 1988-08-10. Applicant: Lasermatic OY. Device class: 2.

Clearance details

Applicant: Lasermatic OY
Product code: Code EWG
Device class: Class 2
Regulation: 21 CFR 874.4500
Advisory panel: Ear, Nose, Throat
Date received: 1987-02-10
Decision date: 1988-08-10
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Finland, FI

Download summary PDF View on FDA.gov ↗

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