FDA 510(k) Application Details - K003761

Device Classification Name Device, Specimen Collection

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510(K) Number K003761
Device Name Device, Specimen Collection
Applicant MEDICAL PACKAGING CORP.
941 AVENIDA ACASO
CAMARILLO, CA 93012-8700 US
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Contact RICHARD CURTIS
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Regulation Number 866.2900

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Classification Product Code LIO
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Date Received 12/06/2000
Decision Date 05/31/2001
Decision SESE - SUBST EQUIV
Classification Advisory Committee MI - Microbiology
Review Advisory Committee MI - Microbiology
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



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