HGM, INC. LASERCATH (STERILE)— 510(k) K860357

Substantially Equivalent

Hgm, Inc.

FDA 510(k) clearance K860357 for HGM, INC. LASERCATH (STERILE), Substantially Equivalent on 1986-04-07. Applicant: Hgm, Inc..

Clearance details

Applicant: Hgm, Inc.
Product code: Code LNK
Advisory panel: General, Plastic Surgery
Date received: 1986-01-30
Decision date: 1986-04-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

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