MEDILAS LASER— 510(k) K833557

Substantially Equivalent

Endo Lase, Inc.

FDA 510(k) clearance K833557 for MEDILAS LASER, Substantially Equivalent on 1984-02-07. Applicant: Endo Lase, Inc..

Clearance details

Applicant: Endo Lase, Inc.
Product code: Code LNK
Advisory panel: General, Plastic Surgery
Date received: 1983-10-07
Decision date: 1984-02-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

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