FDA 510(k) Applications Submitted by RICHARD DESLAURIERS

FDA 510(k) Number Submission Date Device Name Applicant
K990212 01/22/1999 LOCKJAW 15 MINUTE INTERMAXILLARY FIXATION SYSTEM,MODEL LJ100-00 DOCTOR'S RESEARCH GROUP, INC.
K990920 03/18/1999 DRG TITANIUM BONE PLATE DOCTOR'S RESEARCH GROUP, INC.
K991714 05/20/1999 DRG CONVENTIONAL ELECTRONIC DIGITAL STETHOSCOPE, MODEL ECHOP 200-00 DOCTOR'S RESEARCH GROUP, INC.
K981881 05/28/1998 DRG SHERLOCK MF BONE SCREW, COCRMO SELF-TAPPING, TI ALLOY SELF-TAPPING/SELF DRILLING, COCRMO SELF-TAPPING/ SELF DRILLING DOCTOR'S RESEARCH GROUP, INC.
K982169 06/19/1998 SHERLOCK THREADED SUTURE ANCHOR (TIN COATED) DOCTOR'S RESEARCH GROUP, INC.
K012003 06/27/2001 DRG REACTION CHAMBER/SAFETY TIP DOCTOR'S RESEARCH GROUP, INC.
K002047 07/06/2000 DRG PURETONE STETHOSCOPE WITH DRG ANTIMICROBIAL, STETHOSCOPE DIAPHRAGM, MODEL PT2B27(CARDIOLOGY), PT3B27(CLASSIC), PT5B2 DOCTOR'S RESEARCH GROUP, INC.
K012535 08/07/2001 DRG DISPOSABLE VAGINAL SPECULUM DOCTOR'S RESEARCH GROUP, INC.
K142385 08/27/2014 Whisper Pump System Wound RX Medical, LLC
K112684 09/15/2011 MONT BLANC PEDICLE SCREW SYSTEMS QUALGENIX
K112696 09/15/2011 TWIN PEAKS LUMBAR CAGE QUALGENIX LLC
K112801 09/27/2011 AYERS ROCK CERVICAL CAGE QUALGENIX
K112809 09/27/2011 BLUE MOUNTAIN CERVICAL PLATE QUALGENIX LLC
K013786 11/14/2001 DRG ORTHOHEX SS BONE SCREW DOCTOR'S RESEARCH GROUP, INC.
K974817 12/23/1997 DRG MF TITANIUN ALLOY BONE SCREW 1.0MM, 1.2MM, 1.3MM, 1.5MM, 1.7MM, 2.0MM, 2.4MM DOCTOR'S RESEARCH GROUP, INC.


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