MODEL 4900 ND:YAG LASER FOR NEUROSURGERY APPLICA.— 510(k) K880172

Name: FDA 510(k) clearance K880172
Creator: U.S. Food and Drug Administration
Published: 1988-03-11

Substantially Equivalent

Cooper Lasersonics, Inc.

FDA 510(k) clearance K880172 for MODEL 4900 ND:YAG LASER FOR NEUROSURGERY APPLICA., Substantially Equivalent on 1988-03-11. Applicant: Cooper Lasersonics, Inc.. Device class: 3.

Clearance details

Applicant: Cooper Lasersonics, Inc.
Product code: Code LKW
Device class: Class 3
Advisory panel: Unknown
Date received: 1988-01-15
Decision date: 1988-03-11
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.