Drg Reaction Chamber/Safety Tip

No FDA recalls on record, checked 9 Oct 2026.

510(k) Number

K012003 ↗

FDA Product Code

HEI

Device Class

Class II

Regulation

21 CFR Part 884.2660

Advisory Committee

Obstetrics/Gynecology

FDA Decision

SESE Substantially Equivalent

• Drg Titanium Bone Plate

  Class II

  FDA 510(k) K990920 Active Cleared 10 Jun 1999

• Drg Orthohex Ss Bone Screw

  Class II

  FDA 510(k) K013786 Active Cleared 17 Dec 2001

• Kryptonite Bone Cement

  Class II

  FDA 510(k) K091382 Active Cleared 16 Nov 2009

• Drg Puretone Stethoscope with Drg Antimicrobial, Stethoscope Diaphragm, Model PT2B27(Cardiology), PT3B27(Classic), PT5B2

  Class II

  FDA 510(k) K002047 Active Cleared 22 Nov 2000

• DRG Laryngeal Augmentation Implant Device

  Class II

  FDA 510(k) K051487 Active Cleared 22 Dec 2005

• DRG SoftRelease

  Class II

  FDA 510(k) K041018 Active Cleared 18 Oct 2004

See all devices from Doctor'S Research Group, Inc. →