Doctor'S Research Group, Inc.
Doctor'S Research Group, Inc. holds FDA 510(k) medical device clearances, first cleared 1998, most recent 2005.
Top product codes for Doctor'S Research Group, Inc.
Recent clearances by Doctor'S Research Group, Inc.
- K051487 — DRG LARYNGEAL AUGMENTATION IMPLANT DEVICE
- K041018 — DRG SOFTRELEASE
- K012535 — DRG DISPOSABLE VAGINAL SPECULUM
- K012003 — DRG REACTION CHAMBER/SAFETY TIP
- K011736 — DRG QUICKMIX
- K013786 — DRG ORTHOHEX SS BONE SCREW
- K002047 — DRG PURETONE STETHOSCOPE WITH DRG ANTIMICROBIAL, STETHOSCOPE DIAPHRAGM, MODEL PT2B27(CARDIOLOGY), PT3B27(CLASSIC), PT5B2
- K991714 — DRG CONVENTIONAL ELECTRONIC DIGITAL STETHOSCOPE, MODEL ECHOP 200-00
- K990212 — LOCKJAW 15 MINUTE INTERMAXILLARY FIXATION SYSTEM,MODEL LJ100-00
- K990920 — DRG TITANIUM BONE PLATE
- K981881 — DRG SHERLOCK MF BONE SCREW, COCRMO SELF-TAPPING, TI ALLOY SELF-TAPPING/SELF DRILLING, COCRMO SELF-TAPPING/ SELF DRILLING
- K982169 — SHERLOCK THREADED SUTURE ANCHOR (TIN COATED)
- K974817 — DRG MF TITANIUN ALLOY BONE SCREW 1.0MM, 1.2MM, 1.3MM, 1.5MM, 1.7MM, 2.0MM, 2.4MM
Data sourced from openFDA. This site is unofficial and independent of the FDA.