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FDA 510(k) Application Details - K024011
Device Classification Name
Forceps, Biopsy, Electric, Reprocessed
More FDA Info for this Device
510(K) Number
K024011
Device Name
Forceps, Biopsy, Electric, Reprocessed
Applicant
SURGICAL INSTRUMENTS SERVICE AND SAVINGS, INC.
723 CURTIS CT; PO BOX 2060
SISTERS, OR 97759 US
Other 510(k) Applications for this Company
Contact
MARY ANN BARKER
Other 510(k) Applications for this Contact
Regulation Number
876.4300
More FDA Info for this Regulation Number
Classification Product Code
NLU
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
12/04/2002
Decision Date
12/19/2002
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
Y
Expedited Review
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