MODEL 4900 ND:YAG LASER FOR ENDOMETRIAL ABLATION— 510(k) K880173

Name: FDA 510(k) clearance K880173
Creator: U.S. Food and Drug Administration
Published: 1988-03-24

Substantially Equivalent

Cooper Lasersonics, Inc.

FDA 510(k) clearance K880173 for MODEL 4900 ND:YAG LASER FOR ENDOMETRIAL ABLATION, Substantially Equivalent on 1988-03-24. Applicant: Cooper Lasersonics, Inc.. Device class: 2.

Clearance details

Applicant: Cooper Lasersonics, Inc.
Product code: Code HHR
Device class: Class 2
Regulation: 21 CFR 884.4550
Advisory panel: Obstetrics/Gynecology
Date received: 1988-01-15
Decision date: 1988-03-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Santa Clara, CA, US

Download summary PDF View on FDA.gov ↗

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