STEREOMED CAMERA— 510(k) K823534

Name: FDA 510(k) clearance K823534
Creator: U.S. Food and Drug Administration
Published: 1982-12-15

Substantially Equivalent

Diseases of the Skin Clinic, P.A.

FDA 510(k) clearance K823534 for STEREOMED CAMERA, Substantially Equivalent on 1982-12-15. Applicant: Diseases of the Skin Clinic, P.A.. Device class: 1.

Clearance details

Applicant: Diseases of the Skin Clinic, P.A.
Product code: Code FTT
Device class: Class 1
Regulation: 21 CFR 878.4160
Advisory panel: General, Plastic Surgery
Date received: 1982-11-20
Decision date: 1982-12-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

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