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FDA 510(k)

DRG SOFTRELEASE

K-Number: K041018 · 2004-10-18

ApplicantDoctor'S Research Group, Inc.
Decision Date2004-10-18
Product CodeHHT
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

DRG SOFTRELEASE 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 2004-10-18 under 510(k) number K041018. The device is classified under product code HHT. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DRG SOFTRELEASE?

DRG SOFTRELEASE is a medical device that received FDA 510(k) clearance on 2004-10-18. The listed applicant is Doctor'S Research Group, Inc.. The 510(k) number is K041018.

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

DRG SOFTRELEASE received FDA 510(k) clearance on 2004-10-18, under 510(k) number K041018.

Who is the listed applicant for DRG SOFTRELEASE?

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 SOFTRELEASE?

The FDA product code for DRG SOFTRELEASE is HHT.

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

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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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