URITEC TEST STRIP & HUMAN URINE + & - TEST CONTROL— 510(k) K912888

Name: FDA 510(k) clearance K912888
Creator: U.S. Food and Drug Administration
Published: 1992-02-24

Substantially Equivalent

Dynagen, Inc.

FDA 510(k) clearance K912888 for URITEC TEST STRIP & HUMAN URINE + & - TEST CONTROL, Substantially Equivalent on 1992-02-24. Applicant: Dynagen, Inc.. Device class: Unclassified.

Clearance details

Applicant: Dynagen, Inc.
Product code: Code MIG
Device class: Unclassified
Advisory panel: Unknown
Date received: 1991-07-01
Decision date: 1992-02-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cambridge, MA, US

Download summary PDF View on FDA.gov ↗

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