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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