Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

DAHLBERG HEARING AID MODEL MEH

K-Number: K801114 · 1980-05-28

Decision Date1980-05-28
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

DAHLBERG HEARING AID MODEL MEH 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 1980-05-28 under 510(k) number K801114. 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 HEARING AID MODEL MEH?

DAHLBERG HEARING AID MODEL MEH is a medical device that received FDA 510(k) clearance on 1980-05-28. The listed applicant is Dahlberg Electronics, Inc.. The 510(k) number is K801114.

When did DAHLBERG HEARING AID MODEL MEH receive FDA 510(k) clearance?

DAHLBERG HEARING AID MODEL MEH received FDA 510(k) clearance on 1980-05-28, under 510(k) number K801114.

Who is the listed applicant for DAHLBERG HEARING AID MODEL MEH?

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 DAHLBERG HEARING AID MODEL MEH?

The FDA product code for DAHLBERG HEARING AID MODEL MEH 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

View on FDA Database →

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

↑