ENDOCOAGULATOR MODELS 5, 8 & 20 ARGON LASER— 510(k) K870773

Name: FDA 510(k) clearance K870773
Creator: U.S. Food and Drug Administration
Published: 1987-07-10

Substantially Equivalent

Hgm, Inc.

FDA 510(k) clearance K870773 for ENDOCOAGULATOR MODELS 5, 8 & 20 ARGON LASER, Substantially Equivalent on 1987-07-10. Applicant: Hgm, Inc.. Device class: 3.

Clearance details

Applicant: Hgm, Inc.
Product code: Code LLF
Device class: Class 3
Advisory panel: Unknown
Date received: 1987-02-26
Decision date: 1987-07-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LLF

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K864610 — CILAS YM 101 ND:YAG LASER FOR NEUROLOGICAL USE1987-06-18
K860977 — MODEL 545-45 FOR NEUROLOGICAL SURGICAL APPLICATION1986-10-16
K833497 — COOPER MEDICAL MODEL 7701984-04-17

More clearances from Hgm, Inc.

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K950120 — SMART PLUG1995-08-11
K931072 — HGM ILLUMINATING/ASPIRATING ENDOOCULAR PROBE1994-11-10
K931784 — HGM ILLUMINATING IMAGING ENDOCULAR PROBE1994-03-01
K933333 — HGM SCANMAN PLUS1993-09-23
K931499 — Q-11 OPHTHALMIC LASER1993-08-19

Data sourced from openFDA. This site is unofficial and independent of the FDA.