HISTOSET IMMUNOPEROXIDASE TISSURE KIT— 510(k) K820390

Name: FDA 510(k) clearance K820390
Creator: U.S. Food and Drug Administration
Published: 1982-04-14

Substantially Equivalent

Immulok, Inc.

FDA 510(k) clearance K820390 for HISTOSET IMMUNOPEROXIDASE TISSURE KIT, Substantially Equivalent on 1982-04-14. Applicant: Immulok, Inc.. Device class: 1.

Clearance details

Applicant: Immulok, Inc.
Product code: Code LKH
Device class: Class 1
Regulation: 21 CFR 866.3120
Advisory panel: Microbiology
Date received: 1982-02-10
Decision date: 1982-04-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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