CLEARIUM, MOUNTING MEDIUM— 510(k) K830659

Name: FDA 510(k) clearance K830659
Creator: U.S. Food and Drug Administration
Published: 1983-03-17

Substantially Equivalent

Surgipath Medical Industries, Inc.

FDA 510(k) clearance K830659 for CLEARIUM, MOUNTING MEDIUM, Substantially Equivalent on 1983-03-17. Applicant: Surgipath Medical Industries, Inc.. Device class: 1.

Clearance details

Applicant: Surgipath Medical Industries, Inc.
Product code: Code KEP
Device class: Class 1
Regulation: 21 CFR 864.4010
Advisory panel: Pathology
Date received: 1983-03-02
Decision date: 1983-03-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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