SPECIMAN CUP & EMESIS BASIN— 510(k) K792211

Name: FDA 510(k) clearance K792211
Creator: U.S. Food and Drug Administration
Published: 1979-11-16

Substantially Equivalent

General Clinical Plastics Corp.

FDA 510(k) clearance K792211 for SPECIMAN CUP & EMESIS BASIN, Substantially Equivalent on 1979-11-16. Applicant: General Clinical Plastics Corp.. Device class: 1.

Clearance details

Applicant: General Clinical Plastics Corp.
Product code: Code FMH
Device class: Class 1
Regulation: 21 CFR 864.3250
Advisory panel: Pathology
Date received: 1979-11-02
Decision date: 1979-11-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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