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FDA 510(k)

MODEL 344

K-Number: K791506 · 1979-09-19

Decision Date1979-09-19
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

MODEL 344 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 1979-09-19 under 510(k) number K791506. 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 344?

MODEL 344 is a medical device that received FDA 510(k) clearance on 1979-09-19. The listed applicant is Telex Communications, Inc.. The 510(k) number is K791506.

When did MODEL 344 receive FDA 510(k) clearance?

MODEL 344 received FDA 510(k) clearance on 1979-09-19, under 510(k) number K791506.

Who is the listed applicant for MODEL 344?

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 344?

The FDA product code for MODEL 344 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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