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FDA 510(k)

DAHLBERG MODEL AE HIGH FREQUENCY / AID

K-Number: K792278 · 1979-11-30

Decision Date1979-11-30
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

DAHLBERG MODEL AE HIGH FREQUENCY / 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 1979-11-30 under 510(k) number K792278. 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 AE HIGH FREQUENCY / AID?

DAHLBERG MODEL AE HIGH FREQUENCY / AID is a medical device that received FDA 510(k) clearance on 1979-11-30. The listed applicant is Dahlberg Electronics, Inc.. The 510(k) number is K792278.

When did DAHLBERG MODEL AE HIGH FREQUENCY / AID receive FDA 510(k) clearance?

DAHLBERG MODEL AE HIGH FREQUENCY / AID received FDA 510(k) clearance on 1979-11-30, under 510(k) number K792278.

Who is the listed applicant for DAHLBERG MODEL AE HIGH FREQUENCY / 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 MODEL AE HIGH FREQUENCY / AID?

The FDA product code for DAHLBERG MODEL AE HIGH FREQUENCY / 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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