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FDA 510(k)

DAHLBERG MODEL EF BEHIND-THE-EAR HEARING AID

K-Number: K860671 · 1986-04-03

Decision Date1986-04-03
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

DAHLBERG MODEL EF BEHIND-THE-EAR HEARING AID is the device name listed in this FDA 510(k) record. The listed applicant is Miracle-Ear/Dahlberg, Inc.. It received FDA 510(k) clearance on 1986-04-03 under 510(k) number K860671. 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 DAHLBERG MODEL EF BEHIND-THE-EAR HEARING AID?

DAHLBERG MODEL EF BEHIND-THE-EAR HEARING AID is a medical device that received FDA 510(k) clearance on 1986-04-03. The listed applicant is Miracle-Ear/Dahlberg, Inc.. The 510(k) number is K860671.

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

DAHLBERG MODEL EF BEHIND-THE-EAR HEARING AID received FDA 510(k) clearance on 1986-04-03, under 510(k) number K860671.

Who is the listed applicant for DAHLBERG MODEL EF BEHIND-THE-EAR HEARING AID?

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

What is the FDA product code for DAHLBERG MODEL EF BEHIND-THE-EAR HEARING AID?

The FDA product code for DAHLBERG MODEL EF 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 Miracle-Ear/Dahlberg, 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 23 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

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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