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FDA 510(k) Application Details - K021222
Device Classification Name
Powered Laser Surgical Instrument
More FDA Info for this Device
510(K) Number
K021222
Device Name
Powered Laser Surgical Instrument
Applicant
NORWOOD ABBEY , LTD.
5818 PRINCESS CAROLINE PLACE
LEESBURG, FL 34748 US
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Contact
ROBERT HANDREN
Other 510(k) Applications for this Contact
Regulation Number
878.4810
More FDA Info for this Regulation Number
Classification Product Code
GEX
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
04/17/2002
Decision Date
01/08/2003
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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