ENDOCOAGULATOR MODEL 5, 8 & 20 ARGON LASER— 510(k) K871424

Name: FDA 510(k) clearance K871424
Creator: U.S. Food and Drug Administration
Published: 1987-07-08

Substantially Equivalent

Hgm, Inc.

FDA 510(k) clearance K871424 for ENDOCOAGULATOR MODEL 5, 8 & 20 ARGON LASER, Substantially Equivalent on 1987-07-08. Applicant: Hgm, Inc.. Device class: 2.

Clearance details

Applicant: Hgm, Inc.
Product code: Code LMS
Device class: Class 2
Regulation: 21 CFR 874.4490
Advisory panel: Ear, Nose, Throat
Date received: 1987-04-09
Decision date: 1987-07-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

Download summary PDF View on FDA.gov ↗

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K855146 — LASERSCOPE OMNIPLUS PHOTOSURGICAL SYST/ND:YAG OTOL1986-04-11

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K931784 — HGM ILLUMINATING IMAGING ENDOCULAR PROBE1994-03-01
K933333 — HGM SCANMAN PLUS1993-09-23
K931499 — Q-11 OPHTHALMIC LASER1993-08-19

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