MOLECTRON MEDICAL ND:YAG LASER, MODEL 8000— 510(k) K833480

Name: FDA 510(k) clearance K833480
Creator: U.S. Food and Drug Administration
Published: 1983-12-21

Substantially Equivalent

Cooper Lasersonics, Inc.

FDA 510(k) clearance K833480 for MOLECTRON MEDICAL ND:YAG LASER, MODEL 8000, Substantially Equivalent on 1983-12-21. Applicant: Cooper Lasersonics, Inc.. Device class: 2.

Clearance details

Applicant: Cooper Lasersonics, Inc.
Product code: Code LNK
Device class: Class 2
Regulation: 21 CFR 878.4810
Advisory panel: General, Plastic Surgery
Date received: 1983-09-23
Decision date: 1983-12-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Santa Clara, CA, US

Download summary PDF View on FDA.gov ↗

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K880193 — MODEL 4060 N ND:YAG LASER FOR UROLOGICAL USE1988-04-14

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K880429 — ILLUMINA 55 CO2 LASER SYSTEM1988-04-18
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Data sourced from openFDA. This site is unofficial and independent of the FDA.