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FDA 510(k)

PRIZM HEARING SYSTEM

K-Number: K902846 · 1990-10-31

Decision Date1990-10-31
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

PRIZM HEARING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Audioscience, Inc.. It received FDA 510(k) clearance on 1990-10-31 under 510(k) number K902846. 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 PRIZM HEARING SYSTEM?

PRIZM HEARING SYSTEM is a medical device that received FDA 510(k) clearance on 1990-10-31. The listed applicant is Audioscience, Inc.. The 510(k) number is K902846.

When did PRIZM HEARING SYSTEM receive FDA 510(k) clearance?

PRIZM HEARING SYSTEM received FDA 510(k) clearance on 1990-10-31, under 510(k) number K902846.

Who is the listed applicant for PRIZM HEARING SYSTEM?

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

What is the FDA product code for PRIZM HEARING SYSTEM?

The FDA product code for PRIZM HEARING SYSTEM 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 Audioscience, 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

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