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FDA 510(k)

DRG CONVENTIONAL ELECTRONIC DIGITAL STETHOSCOPE, MODEL ECHOP 200-00

K-Number: K991714 · 1999-12-10

ApplicantDoctor'S Research Group, Inc.
Decision Date1999-12-10
Product CodeDQD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DRG CONVENTIONAL ELECTRONIC DIGITAL STETHOSCOPE, MODEL ECHOP 200-00 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 1999-12-10 under 510(k) number K991714. The device is classified under product code DQD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DRG CONVENTIONAL ELECTRONIC DIGITAL STETHOSCOPE, MODEL ECHOP 200-00?

DRG CONVENTIONAL ELECTRONIC DIGITAL STETHOSCOPE, MODEL ECHOP 200-00 is a medical device that received FDA 510(k) clearance on 1999-12-10. The listed applicant is Doctor'S Research Group, Inc.. The 510(k) number is K991714.

When did DRG CONVENTIONAL ELECTRONIC DIGITAL STETHOSCOPE, MODEL ECHOP 200-00 receive FDA 510(k) clearance?

DRG CONVENTIONAL ELECTRONIC DIGITAL STETHOSCOPE, MODEL ECHOP 200-00 received FDA 510(k) clearance on 1999-12-10, under 510(k) number K991714.

Who is the listed applicant for DRG CONVENTIONAL ELECTRONIC DIGITAL STETHOSCOPE, MODEL ECHOP 200-00?

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 CONVENTIONAL ELECTRONIC DIGITAL STETHOSCOPE, MODEL ECHOP 200-00?

The FDA product code for DRG CONVENTIONAL ELECTRONIC DIGITAL STETHOSCOPE, MODEL ECHOP 200-00 is DQD.

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

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Related Devices (Code: DQD)

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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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