MODIFIED CO2 ND:YAG LASER MODEL 880, OB-GYN APPLI.— 510(k) K871220

Name: FDA 510(k) clearance K871220
Creator: U.S. Food and Drug Administration
Published: 1987-07-16

Substantially Equivalent

Cooper Lasersonics, Inc.

FDA 510(k) clearance K871220 for MODIFIED CO2 ND:YAG LASER MODEL 880, OB-GYN APPLI., Substantially Equivalent on 1987-07-16. 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: 1987-03-20
Decision date: 1987-07-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Santa Clara, CA, US

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