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FDA 510(k)

MIRACLE EAR MODEL BP BEHIND-THE-EAR HEARING AID

K-Number: K874830 · 1988-02-17

Decision Date1988-02-17
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

MIRACLE EAR MODEL BP BEHIND-THE-EAR HEARING AID is the device name listed in this FDA 510(k) record. The listed applicant is Dahlberg Electronics, Inc.. It received FDA 510(k) clearance on 1988-02-17 under 510(k) number K874830. 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 MIRACLE EAR MODEL BP BEHIND-THE-EAR HEARING AID?

MIRACLE EAR MODEL BP BEHIND-THE-EAR HEARING AID is a medical device that received FDA 510(k) clearance on 1988-02-17. The listed applicant is Dahlberg Electronics, Inc.. The 510(k) number is K874830.

When did MIRACLE EAR MODEL BP BEHIND-THE-EAR HEARING AID receive FDA 510(k) clearance?

MIRACLE EAR MODEL BP BEHIND-THE-EAR HEARING AID received FDA 510(k) clearance on 1988-02-17, under 510(k) number K874830.

Who is the listed applicant for MIRACLE EAR MODEL BP BEHIND-THE-EAR HEARING AID?

The FDA 510(k) record lists Dahlberg Electronics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MIRACLE EAR MODEL BP BEHIND-THE-EAR HEARING AID?

The FDA product code for MIRACLE EAR MODEL BP BEHIND-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.

Other records listing Dahlberg Electronics, Inc. as applicant

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.

View all 31 devices →

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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