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FDA 510(k)

HEARING AIDS (MODEL E-552 S-712)

K-Number: K761216 · 1976-12-16

Decision Date1976-12-16
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

HEARING AIDS (MODEL E-552 S-712) is the device name listed in this FDA 510(k) record. The listed applicant is Vicon Instrument Co.. It received FDA 510(k) clearance on 1976-12-16 under 510(k) number K761216. The device is classified under product code ESD. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 8 devices →

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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