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


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact