GONOCHEK PANEL— 510(k) K830756

Substantially Equivalent

E-Y Laboratories, Inc.

FDA 510(k) clearance K830756 for GONOCHEK PANEL, Substantially Equivalent on 1983-08-12. Applicant: E-Y Laboratories, Inc.. Device class: 1.

Clearance details

Applicant: E-Y Laboratories, Inc.
Product code: Code JTO
Device class: Class 1
Regulation: 21 CFR 866.2660
Advisory panel: Microbiology
Date received: 1983-03-10
Decision date: 1983-08-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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