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FDA 510(k) Application Details - K993885
Device Classification Name
Electrode, Electrosurgical
More FDA Info for this Device
510(K) Number
K993885
Device Name
Electrode, Electrosurgical
Applicant
LINVATEC CORP.
11311 CONCEPT BLVD.
LARGO, FL 33773-4908 US
Other 510(k) Applications for this Company
Contact
LAURA SENEFF
Other 510(k) Applications for this Contact
Regulation Number
878.4400
More FDA Info for this Regulation Number
Classification Product Code
JOS
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
11/16/1999
Decision Date
02/10/2000
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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