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FDA 510(k) Applications Submitted by JOHN L ROGERS
FDA 510(k) Number
Submission Date
Device Name
Applicant
K961151
03/22/1996
SPINAL NEEDLES
HAKKO SHOJI CO., LTD.
K961152
03/22/1996
TUOHY EPIDURAL NEEDLES
HAKKO SHOJI CO., LTD.
K033144
09/30/2003
DEFIBTECH ELECTRODE ADAPTER, MODEL DAC-300 SERIES
DEFIBTECH, LLC
K033896
12/16/2003
DEFIBTECH AED WITH ATTENUATED DEFIBRILLATION/MONITORING PADS, MODELS DDU-100 WITH DDP-200P
DEFIBTECH, LLC
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