CARBON DIOXIDE (C02) MICROSURGICAL LASER— 510(k) K810562

Name: FDA 510(k) clearance K810562
Creator: U.S. Food and Drug Administration
Published: 1981-03-17

Substantially Equivalent

Metricon, Ltd.

FDA 510(k) clearance K810562 for CARBON DIOXIDE (C02) MICROSURGICAL LASER, Substantially Equivalent on 1981-03-17. Applicant: Metricon, Ltd.. Device class: 2.

Clearance details

Applicant: Metricon, Ltd.
Product code: Code HHR
Device class: Class 2
Regulation: 21 CFR 884.4550
Advisory panel: Obstetrics/Gynecology
Date received: 1981-03-03
Decision date: 1981-03-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, 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 Metricon, Ltd.

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K802355 — METRICON #120 FLUOROPHOTOMETER1980-12-17
K802034 — CO2 MICROSURGICAL LASER SYSTEM #3701980-10-10

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