T UPTAKE ENZYME IMMUNOASSAY CRIMPED TUBE KIT— 510(k) K896925

Substantially Equivalent

In Vitro Diagnostics, Inc.

FDA 510(k) clearance K896925 for T UPTAKE ENZYME IMMUNOASSAY CRIMPED TUBE KIT, Substantially Equivalent on 1990-01-18. Applicant: In Vitro Diagnostics, Inc..

Clearance details

Applicant: In Vitro Diagnostics, Inc.
Product code: Code KHQ
Advisory panel: Clinical Chemistry
Date received: 1989-12-12
Decision date: 1990-01-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Littleton, CO, US

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