ND:YAG SURGICAL LASER FOR GASTRO/UROLOGY APPLICA.— 510(k) K874253

Name: FDA 510(k) clearance K874253
Creator: U.S. Food and Drug Administration
Published: 1988-07-12

Substantially Equivalent

Minnesota Laser Corp.

FDA 510(k) clearance K874253 for ND:YAG SURGICAL LASER FOR GASTRO/UROLOGY APPLICA., Substantially Equivalent on 1988-07-12. Applicant: Minnesota Laser Corp.. Device class: 2.

Clearance details

Applicant: Minnesota Laser Corp.
Product code: Code LNK
Device class: Class 2
Regulation: 21 CFR 878.4810
Advisory panel: General, Plastic Surgery
Date received: 1987-10-20
Decision date: 1988-07-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Minneapolis, MN, US

Download summary PDF View on FDA.gov ↗

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