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FDA 510(k)

E-STETH ELECTRONIC STETHOSCOPE

K-Number: K011898 · 2001-09-14

ApplicantE-Med Innovations, Inc.
Decision Date2001-09-14
Product CodeDQD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

E-STETH ELECTRONIC STETHOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is E-Med Innovations, Inc.. It received FDA 510(k) clearance on 2001-09-14 under 510(k) number K011898. 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 E-STETH ELECTRONIC STETHOSCOPE?

E-STETH ELECTRONIC STETHOSCOPE is a medical device that received FDA 510(k) clearance on 2001-09-14. The listed applicant is E-Med Innovations, Inc.. The 510(k) number is K011898.

When did E-STETH ELECTRONIC STETHOSCOPE receive FDA 510(k) clearance?

E-STETH ELECTRONIC STETHOSCOPE received FDA 510(k) clearance on 2001-09-14, under 510(k) number K011898.

Who is the listed applicant for E-STETH ELECTRONIC STETHOSCOPE?

The FDA 510(k) record lists E-Med Innovations, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for E-STETH ELECTRONIC STETHOSCOPE?

The FDA product code for E-STETH ELECTRONIC STETHOSCOPE is DQD.

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Related Devices (Code: DQD)

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

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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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