HEARING AID, MODEL 783DU
K-Number: K781212 · 1978-08-14
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Device Summary
Frequently Asked Questions
What is the HEARING AID, MODEL 783DU?
HEARING AID, MODEL 783DU is a medical device that received FDA 510(k) clearance on 1978-08-14. The listed applicant is Danavox, Inc.. The 510(k) number is K781212.
When did HEARING AID, MODEL 783DU receive FDA 510(k) clearance?
HEARING AID, MODEL 783DU received FDA 510(k) clearance on 1978-08-14, under 510(k) number K781212.
Who is the listed applicant for HEARING AID, MODEL 783DU?
The FDA 510(k) record lists Danavox, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HEARING AID, MODEL 783DU?
The FDA product code for HEARING AID, MODEL 783DU 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 Danavox, 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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