ACA URINARY PROTEIN ANALYTICAL TEST PACK— 510(k) K822231

Name: FDA 510(k) clearance K822231
Creator: U.S. Food and Drug Administration
Published: 1982-09-30

Substantially Equivalent

E.I. Dupont DE Nemours & Co., Inc.

FDA 510(k) clearance K822231 for ACA URINARY PROTEIN ANALYTICAL TEST PACK, Substantially Equivalent on 1982-09-30. Applicant: E.I. Dupont DE Nemours & Co., Inc.. Device class: 2.

Clearance details

Applicant: E.I. Dupont DE Nemours & Co., Inc.
Product code: Code JGQ
Device class: Class 2
Regulation: 21 CFR 862.1635
Advisory panel: Clinical Chemistry
Date received: 1982-07-27
Decision date: 1982-09-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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