SLT CONTACT ND:YAG LASER FOR INTRA-ABDOM.&GENITAL— 510(k) K872254

Name: FDA 510(k) clearance K872254
Creator: U.S. Food and Drug Administration
Published: 1987-12-14

Substantially Equivalent

Surgical Laser Technologies, Inc.

FDA 510(k) clearance K872254 for SLT CONTACT ND:YAG LASER FOR INTRA-ABDOM.&GENITAL, Substantially Equivalent on 1987-12-14. Applicant: Surgical Laser Technologies, Inc.. Device class: 2.

Clearance details

Applicant: Surgical Laser Technologies, Inc.
Product code: Code HHR
Device class: Class 2
Regulation: 21 CFR 884.4550
Advisory panel: Obstetrics/Gynecology
Date received: 1987-05-20
Decision date: 1987-12-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Malvern, PA, US

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