RESOUND HES, DIGITALLY PROGR., ITE HEARING AID
K-Number: K884871 · 1989-02-22
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Device Summary
Frequently Asked Questions
What is the RESOUND HES, DIGITALLY PROGR., ITE HEARING AID?
RESOUND HES, DIGITALLY PROGR., ITE HEARING AID is a medical device that received FDA 510(k) clearance on 1989-02-22. The listed applicant is Resound Corp.. The 510(k) number is K884871.
When did RESOUND HES, DIGITALLY PROGR., ITE HEARING AID receive FDA 510(k) clearance?
RESOUND HES, DIGITALLY PROGR., ITE HEARING AID received FDA 510(k) clearance on 1989-02-22, under 510(k) number K884871.
Who is the listed applicant for RESOUND HES, DIGITALLY PROGR., ITE HEARING AID?
The FDA 510(k) record lists Resound Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RESOUND HES, DIGITALLY PROGR., ITE HEARING AID?
The FDA product code for RESOUND HES, DIGITALLY PROGR., ITE 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 Resound Corp. 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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