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FDA 510(k) Application Details - K020339
Device Classification Name
Powered Laser Surgical Instrument
More FDA Info for this Device
510(K) Number
K020339
Device Name
Powered Laser Surgical Instrument
Applicant
DORNIER MEDTECH AMERICA, INC.
1155 ROBERTS BLVD.
KENNESAW, GA 30144 US
Other 510(k) Applications for this Company
Contact
Tim Thomas
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
02/01/2002
Decision Date
10/25/2002
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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