SLT CLMD CONTACT LASER— 510(k) K884815

Name: FDA 510(k) clearance K884815
Creator: U.S. Food and Drug Administration
Published: 1988-12-22

Substantially Equivalent

Surgical Laser Technologies, Inc.

FDA 510(k) clearance K884815 for SLT CLMD CONTACT LASER, Substantially Equivalent on 1988-12-22. Applicant: Surgical Laser Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Surgical Laser Technologies, Inc.
Product code: Code LLO
Device class: Class 2
Regulation: 21 CFR 874.4500
Advisory panel: Ear, Nose, Throat
Date received: 1988-11-17
Decision date: 1988-12-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Malvern, PA, US

Download summary PDF View on FDA.gov ↗

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