URINARY ALBUMIN TEST PACK— 510(k) K936202

Name: FDA 510(k) clearance K936202
Creator: U.S. Food and Drug Administration
Published: 1994-05-09

Substantially Equivalent

Dupont Medical Products

FDA 510(k) clearance K936202 for URINARY ALBUMIN TEST PACK, Substantially Equivalent on 1994-05-09. Applicant: Dupont Medical Products. Device class: 1.

Clearance details

Applicant: Dupont Medical Products
Product code: Code JIQ
Device class: Class 1
Regulation: 21 CFR 862.1645
Advisory panel: Clinical Chemistry
Date received: 1993-12-29
Decision date: 1994-05-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wilmington, DE, US

Download summary PDF View on FDA.gov ↗

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