HEARING AIDS (MODEL E-552 S-712)
K-Number: K761216 · 1976-12-16
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Device Summary
Frequently Asked Questions
What is the HEARING AIDS (MODEL E-552 S-712)?
HEARING AIDS (MODEL E-552 S-712) is a medical device that received FDA 510(k) clearance on 1976-12-16. The listed applicant is Vicon Instrument Co.. The 510(k) number is K761216.
When did HEARING AIDS (MODEL E-552 S-712) receive FDA 510(k) clearance?
HEARING AIDS (MODEL E-552 S-712) received FDA 510(k) clearance on 1976-12-16, under 510(k) number K761216.
Who is the listed applicant for HEARING AIDS (MODEL E-552 S-712)?
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 AIDS (MODEL E-552 S-712)?
The FDA product code for HEARING AIDS (MODEL E-552 S-712) 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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