FDA 510(k) Applications Submitted by DOCTOR'S RESEARCH GROUP, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K041018 |
04/20/2004 |
DRG SOFTRELEASE |
DOCTOR'S RESEARCH GROUP, INC. |
| K051487 |
06/06/2005 |
DRG LARYNGEAL AUGMENTATION IMPLANT DEVICE |
DOCTOR'S RESEARCH GROUP, INC. |
| 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. |
| 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. |
| K011736 |
06/05/2001 |
DRG QUICKMIX |
DOCTOR'S RESEARCH GROUP, INC. |
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