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

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..

Clearance details

Applicant: Cooper Lasersonics, Inc.
Product code: Code LKW
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 ↗

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