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)

AUDIO 'D' SOUND SELECTOR POWER (SSP)

K-Number: K964180 · 1996-11-26

Decision Date1996-11-26
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

AUDIO 'D' SOUND SELECTOR POWER (SSP) is the device name listed in this FDA 510(k) record. The listed applicant is Hearing Solutions, Inc.. It received FDA 510(k) clearance on 1996-11-26 under 510(k) number K964180. 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 AUDIO 'D' SOUND SELECTOR POWER (SSP)?

AUDIO 'D' SOUND SELECTOR POWER (SSP) is a medical device that received FDA 510(k) clearance on 1996-11-26. The listed applicant is Hearing Solutions, Inc.. The 510(k) number is K964180.

When did AUDIO 'D' SOUND SELECTOR POWER (SSP) receive FDA 510(k) clearance?

AUDIO 'D' SOUND SELECTOR POWER (SSP) received FDA 510(k) clearance on 1996-11-26, under 510(k) number K964180.

Who is the listed applicant for AUDIO 'D' SOUND SELECTOR POWER (SSP)?

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

What is the FDA product code for AUDIO 'D' SOUND SELECTOR POWER (SSP)?

The FDA product code for AUDIO 'D' SOUND SELECTOR POWER (SSP) 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 Hearing Solutions, 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.

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.

↑