HEARING AID, S-522 FM
K-Number: K760215 · 1976-07-21
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Device Summary
Frequently Asked Questions
What is the HEARING AID, S-522 FM?
HEARING AID, S-522 FM is a medical device that received FDA 510(k) clearance on 1976-07-21. The listed applicant is Vicon Instrument Co.. The 510(k) number is K760215.
When did HEARING AID, S-522 FM receive FDA 510(k) clearance?
HEARING AID, S-522 FM received FDA 510(k) clearance on 1976-07-21, under 510(k) number K760215.
Who is the listed applicant for HEARING AID, S-522 FM?
The FDA 510(k) record lists Vicon Instrument Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HEARING AID, S-522 FM?
The FDA product code for HEARING AID, S-522 FM 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 Vicon Instrument Co. 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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