DAHLBERG # AF BEHING THE EAR HEARING/AID
K-Number: K800181 · 1980-02-28
Advertisement
Device Summary
Frequently Asked Questions
What is the DAHLBERG # AF BEHING THE EAR HEARING/AID?
DAHLBERG # AF BEHING THE EAR HEARING/AID is a medical device that received FDA 510(k) clearance on 1980-02-28. The listed applicant is Dahlberg Electronics, Inc.. The 510(k) number is K800181.
When did DAHLBERG # AF BEHING THE EAR HEARING/AID receive FDA 510(k) clearance?
DAHLBERG # AF BEHING THE EAR HEARING/AID received FDA 510(k) clearance on 1980-02-28, under 510(k) number K800181.
Who is the listed applicant for DAHLBERG # AF BEHING 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 DAHLBERG # AF BEHING THE EAR HEARING/AID?
The FDA product code for DAHLBERG # AF BEHING 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.
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.
Advertisement