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FDA 510(k) Application Details - K024120
Device Classification Name
Kit, Needle, Biopsy
More FDA Info for this Device
510(K) Number
K024120
Device Name
Kit, Needle, Biopsy
Applicant
ALLEGIANCE HEALTHCARE CORP.
1500 WAUKEGAN RD. MPWM-1E
MCGAW PARK, IL 60085 US
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Contact
SHARON NICHOLS
Other 510(k) Applications for this Contact
Regulation Number
876.1075
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Classification Product Code
FCG
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More FDA Info for this Product Code
Date Received
12/16/2002
Decision Date
01/15/2003
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
GU - Gastroenterology & Urology
Review Advisory Committee
GU - Gastroenterology & Urology
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
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