DRG QUICKMIX— 510(k) K011736

Substantially Equivalent

Doctor'S Research Group, Inc.

FDA 510(k) clearance K011736 for DRG QUICKMIX, Substantially Equivalent on 2002-01-30. Applicant: Doctor'S Research Group, Inc.. Device class: 2.

Clearance details

Applicant: Doctor'S Research Group, Inc.
Product code: Code GXP
Device class: Class 2
Regulation: 21 CFR 882.5300
Advisory panel: Neurology
Date received: 2001-06-05
Decision date: 2002-01-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wolcott, CT, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code GXP

K251959 — TnR Cranial Implant2026-07-30
K261265 — Permatage XT Settable Bone Putty2026-06-15
K253732 — Permatage Flowable, Settable Bone Paste2026-03-13
K253854 — MONTAGE XT Cranial Cement2026-01-02
K241027 — Permatage Settable Bone Putty2024-09-26

More clearances from Doctor'S Research Group, Inc.

K051487 — DRG LARYNGEAL AUGMENTATION IMPLANT DEVICE2005-12-22
K041018 — DRG SOFTRELEASE2004-10-18
K012535 — DRG DISPOSABLE VAGINAL SPECULUM2002-03-01
K012003 — DRG REACTION CHAMBER/SAFETY TIP2002-02-12
K013786 — DRG ORTHOHEX SS BONE SCREW2001-12-17

Data sourced from openFDA. This site is unofficial and independent of the FDA.