COOPER LASERSONICS, 8000 ND.YAGLASER— 510(k) K841869

Name: FDA 510(k) clearance K841869
Creator: U.S. Food and Drug Administration
Published: 1984-08-08

Substantially Equivalent

Cooper Lasersonics, Inc.

FDA 510(k) clearance K841869 for COOPER LASERSONICS, 8000 ND.YAGLASER, Substantially Equivalent on 1984-08-08. Applicant: Cooper Lasersonics, Inc.. Device class: 2.

Clearance details

Applicant: Cooper Lasersonics, Inc.
Product code: Code LNK
Device class: Class 2
Regulation: 21 CFR 878.4810
Advisory panel: General, Plastic Surgery
Date received: 1984-05-04
Decision date: 1984-08-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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