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FDA 510(k)

DRG QUICKMIX

K-Number: K011736 · 2002-01-30

ApplicantDoctor'S Research Group, Inc.
Decision Date2002-01-30
Product CodeGXP
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

DRG QUICKMIX is the device name listed in this FDA 510(k) record. The listed applicant is Doctor'S Research Group, Inc.. It received FDA 510(k) clearance on 2002-01-30 under 510(k) number K011736. The device is classified under product code GXP. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DRG QUICKMIX?

DRG QUICKMIX is a medical device that received FDA 510(k) clearance on 2002-01-30. The listed applicant is Doctor'S Research Group, Inc.. The 510(k) number is K011736.

When did DRG QUICKMIX receive FDA 510(k) clearance?

DRG QUICKMIX received FDA 510(k) clearance on 2002-01-30, under 510(k) number K011736.

Who is the listed applicant for DRG QUICKMIX?

The FDA 510(k) record lists Doctor'S Research Group, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DRG QUICKMIX?

The FDA product code for DRG QUICKMIX is GXP.

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Other records listing Doctor'S Research Group, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K051487DRG LARYNGEAL AUGMENTATION IMPLANT DEVICEK041018DRG SOFTRELEASEK012535DRG DISPOSABLE VAGINAL SPECULUMK012003DRG REACTION CHAMBER/SAFETY TIPK013786DRG ORTHOHEX SS BONE SCREWK002047DRG PURETONE STETHOSCOPE WITH DRG ANTIMICROBIAL, STETHOSCOPE DIAPHRAGM, MODEL PT2B27(CARDIOLOGY), PT3B27(CLASSIC), PT5B2

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Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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