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 695D, 905 & 960P)

K-Number: K760996 · 1976-11-16

Decision Date1976-11-16
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

HEARING AID (MODEL 695D, 905 & 960P) is the device name listed in this FDA 510(k) record. The listed applicant is Unitron Industries, Inc.. It received FDA 510(k) clearance on 1976-11-16 under 510(k) number K760996. 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 695D, 905 & 960P)?

HEARING AID (MODEL 695D, 905 & 960P) is a medical device that received FDA 510(k) clearance on 1976-11-16. The listed applicant is Unitron Industries, Inc.. The 510(k) number is K760996.

When did HEARING AID (MODEL 695D, 905 & 960P) receive FDA 510(k) clearance?

HEARING AID (MODEL 695D, 905 & 960P) received FDA 510(k) clearance on 1976-11-16, under 510(k) number K760996.

Who is the listed applicant for HEARING AID (MODEL 695D, 905 & 960P)?

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

What is the FDA product code for HEARING AID (MODEL 695D, 905 & 960P)?

The FDA product code for HEARING AID (MODEL 695D, 905 & 960P) 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 Unitron Industries, 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 69 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.

↑