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FDA 510(k)

VIBRASOUND IN-THE-EAR HEARING AID

K-Number: K880184 · 1988-03-09

Decision Date1988-03-09
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

VIBRASOUND IN-THE-EAR HEARING AID is the device name listed in this FDA 510(k) record. The listed applicant is Vibrasound Research Corp.. It received FDA 510(k) clearance on 1988-03-09 under 510(k) number K880184. The device is classified under product code ESD. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIBRASOUND IN-THE-EAR HEARING AID?

VIBRASOUND IN-THE-EAR HEARING AID is a medical device that received FDA 510(k) clearance on 1988-03-09. The listed applicant is Vibrasound Research Corp.. The 510(k) number is K880184.

When did VIBRASOUND IN-THE-EAR HEARING AID receive FDA 510(k) clearance?

VIBRASOUND IN-THE-EAR HEARING AID received FDA 510(k) clearance on 1988-03-09, under 510(k) number K880184.

Who is the listed applicant for VIBRASOUND IN-THE-EAR HEARING AID?

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

What is the FDA product code for VIBRASOUND IN-THE-EAR HEARING AID?

The FDA product code for VIBRASOUND IN-THE-EAR HEARING AID is ESD.

Related Clinical Trials

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.

Related Devices (Code: ESD)

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.

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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