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FDA 510(k)

MODEL 363C HEARING AID

K-Number: K844648 · 1985-01-07

Decision Date1985-01-07
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

MODEL 363C HEARING AID is the device name listed in this FDA 510(k) record. The listed applicant is Telex Communications, Inc.. It received FDA 510(k) clearance on 1985-01-07 under 510(k) number K844648. 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 MODEL 363C HEARING AID?

MODEL 363C HEARING AID is a medical device that received FDA 510(k) clearance on 1985-01-07. The listed applicant is Telex Communications, Inc.. The 510(k) number is K844648.

When did MODEL 363C HEARING AID receive FDA 510(k) clearance?

MODEL 363C HEARING AID received FDA 510(k) clearance on 1985-01-07, under 510(k) number K844648.

Who is the listed applicant for MODEL 363C HEARING AID?

The FDA 510(k) record lists Telex Communications, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL 363C HEARING AID?

The FDA product code for MODEL 363C 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 Telex Communications, 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.

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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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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