KELLEY-PLUS WITH MEASURETTE— 510(k) K790053

Name: FDA 510(k) clearance K790053
Creator: U.S. Food and Drug Administration
Published: 1979-01-26

Substantially Equivalent

John N. Haswell, M.D.

FDA 510(k) clearance K790053 for KELLEY-PLUS WITH MEASURETTE, Substantially Equivalent on 1979-01-26. Applicant: John N. Haswell, M.D.. Device class: 2.

Clearance details

Applicant: John N. Haswell, M.D.
Product code: Code KKX
Device class: Class 2
Regulation: 21 CFR 878.4370
Advisory panel: General, Plastic Surgery
Date received: 1979-01-09
Decision date: 1979-01-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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