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 AID MODEL 337D

K-Number: K853264 · 1985-09-23

Decision Date1985-09-23
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

HEARING AID MODEL 337D 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 1985-09-23 under 510(k) number K853264. 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 AID MODEL 337D?

HEARING AID MODEL 337D is a medical device that received FDA 510(k) clearance on 1985-09-23. The listed applicant is Telex Communications, Inc.. The 510(k) number is K853264.

When did HEARING AID MODEL 337D receive FDA 510(k) clearance?

HEARING AID MODEL 337D received FDA 510(k) clearance on 1985-09-23, under 510(k) number K853264.

Who is the listed applicant for HEARING AID MODEL 337D?

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 AID MODEL 337D?

The FDA product code for HEARING AID MODEL 337D 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.

↑