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FDA 510(k) Application Details - K030480
Device Classification Name
Powered Laser Surgical Instrument
More FDA Info for this Device
510(K) Number
K030480
Device Name
Powered Laser Surgical Instrument
Applicant
A&M TECHNOLOGY
28, RUE DE LA TREMOILLE
PARIS F 75008 FR
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Contact
PASCAL DANET
Other 510(k) Applications for this Contact
Regulation Number
878.4810
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Classification Product Code
GEX
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More FDA Info for this Product Code
Date Received
02/13/2003
Decision Date
05/14/2003
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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