Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

HEARING AIDS 372 & 372 AI

K-Number: K843068 · 1984-12-03

Decision Date1984-12-03
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

HEARING AIDS 372 & 372 AI 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 1984-12-03 under 510(k) number K843068. 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 372 & 372 AI?

HEARING AIDS 372 & 372 AI is a medical device that received FDA 510(k) clearance on 1984-12-03. The listed applicant is Telex Communications, Inc.. The 510(k) number is K843068.

When did HEARING AIDS 372 & 372 AI receive FDA 510(k) clearance?

HEARING AIDS 372 & 372 AI received FDA 510(k) clearance on 1984-12-03, under 510(k) number K843068.

Who is the listed applicant for HEARING AIDS 372 & 372 AI?

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 HEARING AIDS 372 & 372 AI?

The FDA product code for HEARING AIDS 372 & 372 AI 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.

View all 50 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.

↑