DAHLBERG MODEL AM
K-Number: K811226 · 1981-05-13
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Device Summary
Frequently Asked Questions
What is the DAHLBERG MODEL AM?
DAHLBERG MODEL AM is a medical device that received FDA 510(k) clearance on 1981-05-13. The listed applicant is Dahlberg Electronics, Inc.. The 510(k) number is K811226.
When did DAHLBERG MODEL AM receive FDA 510(k) clearance?
DAHLBERG MODEL AM received FDA 510(k) clearance on 1981-05-13, under 510(k) number K811226.
Who is the listed applicant for DAHLBERG MODEL AM?
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 AM?
The FDA product code for DAHLBERG MODEL AM 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.
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