SDI PREPAX DILUKIT HW— 510(k) K840041

Name: FDA 510(k) clearance K840041
Creator: U.S. Food and Drug Administration
Published: 1984-03-05

Substantially Equivalent

Scientific Distributors, Inc.

FDA 510(k) clearance K840041 for SDI PREPAX DILUKIT HW, Substantially Equivalent on 1984-03-05. Applicant: Scientific Distributors, Inc.. Device class: 1.

Clearance details

Applicant: Scientific Distributors, Inc.
Product code: Code GIF
Device class: Class 1
Regulation: 21 CFR 864.8200
Advisory panel: Hematology
Date received: 1984-01-06
Decision date: 1984-03-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.