MODEL 8 & 20 ARGON LASER FOR PELVIC SURGERY IN GYN— 510(k) K862227

Name: FDA 510(k) clearance K862227
Creator: U.S. Food and Drug Administration
Published: 1986-08-19

Substantially Equivalent

Hgm, Inc.

FDA 510(k) clearance K862227 for MODEL 8 & 20 ARGON LASER FOR PELVIC SURGERY IN GYN, Substantially Equivalent on 1986-08-19. Applicant: Hgm, Inc.. Device class: 2.

Clearance details

Applicant: Hgm, Inc.
Product code: Code HHR
Device class: Class 2
Regulation: 21 CFR 884.4550
Advisory panel: Obstetrics/Gynecology
Date received: 1986-06-11
Decision date: 1986-08-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HHR

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K881507 — ENDOCOAGULATOR MODEL 20 LASER & ACCESSORIES1989-04-27
K871875 — MODEL 5050 SURGILASER FOR OB-GYN USE1988-08-22
K875314 — GL-35 COLPOSCOPIC LASER SYSTEM1988-08-05
K874615 — LASER CANNISTER FILTER1988-06-23
K880591 — LASEGUIDE 600A, 600B, 400A, 400B FOR OB-GYN USE1988-06-01

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

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