CILAS YM 101 ND:YAG LASER FOR NEUROLOGICAL USE— 510(k) K864610

Name: FDA 510(k) clearance K864610
Creator: U.S. Food and Drug Administration
Published: 1987-06-18

Substantially Equivalent

Inframed, Inc.

FDA 510(k) clearance K864610 for CILAS YM 101 ND:YAG LASER FOR NEUROLOGICAL USE, Substantially Equivalent on 1987-06-18. Applicant: Inframed, Inc.. Device class: 3.

Clearance details

Applicant: Inframed, Inc.
Product code: Code LLF
Device class: Class 3
Advisory panel: Unknown
Date received: 1986-11-20
Decision date: 1987-06-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Needham, MA, US

Download summary PDF View on FDA.gov ↗

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