LEIF CENTRIFUGAL CYTOLOGY BUCKET— 510(k) K792032

Name: FDA 510(k) clearance K792032
Creator: U.S. Food and Drug Administration
Published: 1979-11-30

Substantially Equivalent

Robert C. Leif, Ph.D.

FDA 510(k) clearance K792032 for LEIF CENTRIFUGAL CYTOLOGY BUCKET, Substantially Equivalent on 1979-11-30. Applicant: Robert C. Leif, Ph.D.. Device class: 1.

Clearance details

Applicant: Robert C. Leif, Ph.D.
Product code: Code IFB
Device class: Class 1
Regulation: 21 CFR 864.3300
Advisory panel: Pathology
Date received: 1979-10-10
Decision date: 1979-11-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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