Doctor'S Research Group, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 13
- Inspections
- 1
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K051487 | DRG LARYNGEAL AUGMENTATION IMPLANT DEVICE | December 22, 2005 |
| K041018 | DRG SOFTRELEASE | October 18, 2004 |
| K012535 | DRG DISPOSABLE VAGINAL SPECULUM | March 1, 2002 |
| K012003 | DRG REACTION CHAMBER/SAFETY TIP | February 12, 2002 |
| K011736 | DRG QUICKMIX | January 30, 2002 |
| K013786 | DRG ORTHOHEX SS BONE SCREW | December 17, 2001 |
| K002047 | DRG PURETONE STETHOSCOPE WITH DRG ANTIMICROBIAL, STETHOSCOPE DIAPHRAGM, MODEL PT2B27(CARDIOLOGY), PT | November 22, 2000 |
| K991714 | DRG CONVENTIONAL ELECTRONIC DIGITAL STETHOSCOPE, MODEL ECHOP 200-00 | December 10, 1999 |
| K990212 | LOCKJAW 15 MINUTE INTERMAXILLARY FIXATION SYSTEM,MODEL LJ100-00 | September 14, 1999 |
| K990920 | DRG TITANIUM BONE PLATE | June 10, 1999 |
| K981881 | DRG SHERLOCK MF BONE SCREW, COCRMO SELF-TAPPING, TI ALLOY SELF-TAPPING/SELF DRILLING, COCRMO SELF-TA | December 2, 1998 |
| K982169 | SHERLOCK THREADED SUTURE ANCHOR (TIN COATED) | September 14, 1998 |
| K974817 | DRG MF TITANIUN ALLOY BONE SCREW 1.0MM, 1.2MM, 1.3MM, 1.5MM, 1.7MM, 2.0MM, 2.4MM | March 13, 1998 |