DU PONT ACA NEV/EEV VERIFIER— 510(k) K930501

Name: FDA 510(k) clearance K930501
Creator: U.S. Food and Drug Administration
Published: 1993-08-09

Substantially Equivalent

Dupont Medical Products

FDA 510(k) clearance K930501 for DU PONT ACA NEV/EEV VERIFIER, Substantially Equivalent on 1993-08-09. Applicant: Dupont Medical Products. Device class: 2.

Clearance details

Applicant: Dupont Medical Products
Product code: Code JIS
Device class: Class 2
Regulation: 21 CFR 862.1150
Advisory panel: Clinical Chemistry
Date received: 1993-02-01
Decision date: 1993-08-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wilmington, DE, US

Download summary PDF View on FDA.gov ↗

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