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FDA 510(k) Application Details - K962371
Device Classification Name
Dermatome
More FDA Info for this Device
510(K) Number
K962371
Device Name
Dermatome
Applicant
DSP WORLDWIDE
49 PLAIN ST.
NORTH ATTLEBORO, MA 02760 US
Other 510(k) Applications for this Company
Contact
ROSINA ROBINSON
Other 510(k) Applications for this Contact
Regulation Number
878.4820
More FDA Info for this Regulation Number
Classification Product Code
GFD
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
06/19/1996
Decision Date
08/29/1996
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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