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FDA 510(k) Application Details - K974594
Device Classification Name
Forceps
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510(K) Number
K974594
Device Name
Forceps
Applicant
TITAN MFG., INC.
6 JAMIE LN.
PHOENIXVILLE, PA 19460 US
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Contact
DONALD SEAVEY
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Regulation Number
878.4800
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Classification Product Code
HTD
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More FDA Info for this Product Code
Date Received
12/09/1997
Decision Date
06/24/1998
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
SU - General & Plastic Surgery
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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