Doctor'S Research Group, Inc.
FDA 510(k) & PMA Approved Devices — 13 products
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Total Devices13
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K051487 | DRG LARYNGEAL AUGMENTATION IMPLANT DEVICE | KHJ | 2005-12-22 | View |
| 510(k) | K041018 | DRG SOFTRELEASE | HHT | 2004-10-18 | View |
| 510(k) | K012535 | DRG DISPOSABLE VAGINAL SPECULUM | HIB | 2002-03-01 | View |
| 510(k) | K012003 | DRG REACTION CHAMBER/SAFETY TIP | HEI | 2002-02-12 | View |
| 510(k) | K011736 | DRG QUICKMIX | GXP | 2002-01-30 | View |
| 510(k) | K013786 | DRG ORTHOHEX SS BONE SCREW | HWC | 2001-12-17 | View |
| 510(k) | K002047 | DRG PURETONE STETHOSCOPE WITH DRG ANTIMICROBIAL, STETHOSCOPE DIAPHRAGM, MODEL PT2B27(CARDIOLOGY), PT3B27(CLASSIC), PT5B2 | DQD | 2000-11-22 | View |
| 510(k) | K991714 | DRG CONVENTIONAL ELECTRONIC DIGITAL STETHOSCOPE, MODEL ECHOP 200-00 | DQD | 1999-12-10 | View |
| 510(k) | K990212 | LOCKJAW 15 MINUTE INTERMAXILLARY FIXATION SYSTEM,MODEL LJ100-00 | DYX | 1999-09-14 | View |
| 510(k) | K990920 | DRG TITANIUM BONE PLATE | JEY | 1999-06-10 | View |
| 510(k) | K981881 | DRG SHERLOCK MF BONE SCREW, COCRMO SELF-TAPPING, TI ALLOY SELF-TAPPING/SELF DRILLING, COCRMO SELF-TAPPING/ SELF DRILLING | DZL | 1998-12-02 | View |
| 510(k) | K982169 | SHERLOCK THREADED SUTURE ANCHOR (TIN COATED) | MBI | 1998-09-14 | View |
| 510(k) | K974817 | DRG MF TITANIUN ALLOY BONE SCREW 1.0MM, 1.2MM, 1.3MM, 1.5MM, 1.7MM, 2.0MM, 2.4MM | DZL | 1998-03-13 | View |
No matching devices.
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