FDA 510(k) Applications Submitted by STEVEN CHERNOFF

FDA 510(k) Number Submission Date Device Name Applicant
K030346 02/03/2003 TWINHEADS TH-101 EXTRACORPOREAL SHOCK WAVE LITHOTRIPTER FMD, LLC
K130952 04/05/2013 PRECISION ONE LIFECARE; DETECTO; DETECTO PRECISION ONE LIFECARE, LTD.
K050883 04/07/2005 SAFERSLEEP SYSTEM SAFER SLEEP LLC
K062325 08/09/2006 RS-4I MUSCLE STIMULATOR FAMILY RS MEDICAL
K053481 12/14/2005 KELO-COTE SPRAY ADVANCED BIO-TECHNOLOGIES, INC.


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