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FDA 510(k) Application Details - K971317
Device Classification Name
Kit, Surgical Instrument, Disposable
More FDA Info for this Device
510(K) Number
K971317
Device Name
Kit, Surgical Instrument, Disposable
Applicant
NATIONAL HEALTHCARE MFG. CORP.
49 PLAIN ST.
NORTH ATTLEBORO, MA 02760 US
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Contact
CAROLANN KOTULA
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Regulation Number
878.4800
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Classification Product Code
KDD
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More FDA Info for this Product Code
Date Received
04/09/1997
Decision Date
05/08/1997
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
SU - General & Plastic Surgery
Review Advisory Committee
SU - General & Plastic Surgery
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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