ACON QUIK-CHECK II MIDSTREAM HOME PREGNANCY TEST— 510(k) K032510

Substantially Equivalent

ACON Laboratories, Inc.

FDA 510(k) clearance K032510 for ACON QUIK-CHECK II MIDSTREAM HOME PREGNANCY TEST, Substantially Equivalent on 2003-09-22. Applicant: ACON Laboratories, Inc..

Clearance details

Applicant: ACON Laboratories, Inc.
Product code: Code LCX
Advisory panel: Clinical Chemistry
Date received: 2003-08-14
Decision date: 2003-09-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

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