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FDA 510(k) Applications Submitted by Mark Smutka
FDA 510(k) Number
Submission Date
Device Name
Applicant
K070443
02/15/2007
INTRACEPT BI-POLAR RF PROBE, MODEL 04814
RELIEVANT MEDSYSTEMS, INC.
K111284
05/06/2011
FLASH-C PTCA BALLOON DILATION CATHETER - 5MM X 19MM X 135CM / 6MM X 19MM X 135CM
OSTIAL CORPORATION
K981870
05/28/1998
VISAGE COSMETIC SURGERY SYSTEM
ARTHROCARE CORP.
K973478
09/15/1997
ARTHROCARE SINUS ELECTROSURGERY SYSTEM
ARTHROCARE CORP.
K083856
12/24/2008
INTRACEPT FLEXIBLE BI-POLAR RF PROBE AND CURVED INSTRUMENT SET, MODELS: FG0018, FG0026
RELIEVANT MEDSYSTEMS, INC.
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