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FDA 510(k) Application Details - K020024
Device Classification Name
Instrument, Biopsy
More FDA Info for this Device
510(K) Number
K020024
Device Name
Instrument, Biopsy
Applicant
ARTEMIS MEDICAL, INC.
21021 CORSAIR BLVD.
HAYWARD, CA 94545 US
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Contact
ALLAN L ABATI
Other 510(k) Applications for this Contact
Regulation Number
876.1075
More FDA Info for this Regulation Number
Classification Product Code
KNW
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
01/03/2002
Decision Date
04/03/2002
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
GU - Gastroenterology & Urology
Review Advisory Committee
GU - Gastroenterology & Urology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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