MODEL 5050 SURGILASER FOR UROLOGY USE— 510(k) K871932

Substantially Equivalent

Lasermatic, Inc.

FDA 510(k) clearance K871932 for MODEL 5050 SURGILASER FOR UROLOGY USE, Substantially Equivalent on 1988-03-25. Applicant: Lasermatic, Inc..

Clearance details

Applicant: Lasermatic, Inc.
Product code: Code LNK
Advisory panel: General, Plastic Surgery
Date received: 1987-05-19
Decision date: 1988-03-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Dallas, TX, US

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