DUPONT DIMENSION TOTAL PROTEIN METHOD— 510(k) K950920

Name: FDA 510(k) clearance K950920
Creator: U.S. Food and Drug Administration
Published: 1995-08-11

Substantially Equivalent

Dupont Medical Products

FDA 510(k) clearance K950920 for DUPONT DIMENSION TOTAL PROTEIN METHOD, Substantially Equivalent on 1995-08-11. Applicant: Dupont Medical Products. Device class: 2.

Clearance details

Applicant: Dupont Medical Products
Product code: Code CEK
Device class: Class 2
Regulation: 21 CFR 862.1635
Advisory panel: Clinical Chemistry
Date received: 1995-03-01
Decision date: 1995-08-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wilmington, DE, US

Download summary PDF View on FDA.gov ↗

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K961864 — CSF/URINE TOTAL PROTEIN1996-10-24

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