MINUTEMAN CO2 MICROSURGICAL LASER GYN— 510(k) K843515

Name: FDA 510(k) clearance K843515
Creator: U.S. Food and Drug Administration
Published: 1985-02-04

Substantially Equivalent

American Surgical Laser, Inc.

FDA 510(k) clearance K843515 for MINUTEMAN CO2 MICROSURGICAL LASER GYN, Substantially Equivalent on 1985-02-04. Applicant: American Surgical Laser, Inc.. Device class: 2.

Clearance details

Applicant: American Surgical Laser, Inc.
Product code: Code HHR
Device class: Class 2
Regulation: 21 CFR 884.4550
Advisory panel: Obstetrics/Gynecology
Date received: 1984-09-05
Decision date: 1985-02-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Woburn, MA, 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 American Surgical Laser, Inc.

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K843517 — MINUTEMAN CO2 MICROSURG LASER DERMATOL-1984-12-07
K843518 — MINUTEMAN C02 MICROSURG LASER PODIATRY1984-12-07
K843519 — MINUTEMAN CO2 MICROSURG LASER GEN SURG1984-12-07
K843514 — MINUTEMAN CO2 MICROSURGICAL LASER OTO1984-12-04

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