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FDA 510(k) Application Details - K051300
Device Classification Name
Holder, Infant Position
More FDA Info for this Device
510(K) Number
K051300
Device Name
Holder, Infant Position
Applicant
KAMBER CORPORATION
1301 K STREET, N.W.
SUITE 1100 - EAST TOWER
WASHINGTON, DC 20005-3373 US
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Contact
DAVID J BLOCH
Other 510(k) Applications for this Contact
Regulation Number
880.5680
More FDA Info for this Regulation Number
Classification Product Code
FRP
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More FDA Info for this Product Code
Date Received
05/18/2005
Decision Date
12/08/2005
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
HO - General Hospital
Review Advisory Committee
HO - General Hospital
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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