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

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K002047 ↗

FDA Product Code

DQD

Models / Variants

PT2B27(Cardiology)

PT3B27(Classic)

PT5B2

Device Class

Class II

Regulation

21 CFR Part 870.1875

Advisory Committee

Cardiovascular

FDA Decision

SESE Substantially Equivalent

• Drg Reaction Chamber/Safety Tip

  Class II

  FDA 510(k) K012003 Active Cleared 12 Feb 2002

• 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 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

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