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

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..

Clearance details

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

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