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FDA 510(k)

ESTATION ELECTRONIC STETHOSCOPE, MODEL DR200

K-Number: K001788 · 2000-11-03

ApplicantErecords Enterprises
Decision Date2000-11-03
Product CodeDQD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ESTATION ELECTRONIC STETHOSCOPE, MODEL DR200 is the device name listed in this FDA 510(k) record. The listed applicant is Erecords Enterprises. It received FDA 510(k) clearance on 2000-11-03 under 510(k) number K001788. 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 ESTATION ELECTRONIC STETHOSCOPE, MODEL DR200?

ESTATION ELECTRONIC STETHOSCOPE, MODEL DR200 is a medical device that received FDA 510(k) clearance on 2000-11-03. The listed applicant is Erecords Enterprises. The 510(k) number is K001788.

When did ESTATION ELECTRONIC STETHOSCOPE, MODEL DR200 receive FDA 510(k) clearance?

ESTATION ELECTRONIC STETHOSCOPE, MODEL DR200 received FDA 510(k) clearance on 2000-11-03, under 510(k) number K001788.

Who is the listed applicant for ESTATION ELECTRONIC STETHOSCOPE, MODEL DR200?

The FDA 510(k) record lists Erecords Enterprises as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ESTATION ELECTRONIC STETHOSCOPE, MODEL DR200?

The FDA product code for ESTATION ELECTRONIC STETHOSCOPE, MODEL DR200 is DQD.

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Related Devices (Code: DQD)

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Official Source

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

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