DIAGNOSTIC KIT, FERRITAB-FE-59— 510(k) K782159

Name: FDA 510(k) clearance K782159
Creator: U.S. Food and Drug Administration
Published: 1979-02-01

Substantially Equivalent

Leeco Diagnostics, Inc.

FDA 510(k) clearance K782159 for DIAGNOSTIC KIT, FERRITAB-FE-59, Substantially Equivalent on 1979-02-01. Applicant: Leeco Diagnostics, Inc.. Device class: 1.

Clearance details

Applicant: Leeco Diagnostics, Inc.
Product code: Code JJA
Device class: Class 1
Regulation: 21 CFR 862.1410
Advisory panel: Clinical Chemistry
Date received: 1978-12-22
Decision date: 1979-02-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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