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FDA 510(k) Application Details - K003761
Device Classification Name
Device, Specimen Collection
More FDA Info for this Device
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
Other 510(k) Applications for this Contact
Regulation Number
866.2900
More FDA Info for this Regulation Number
Classification Product Code
LIO
Other 510(k) Applications for this Device
More FDA Info for this Product Code
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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