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FDA 510(k)

ITE HEARING AID MODEL PALOMINO

K-Number: K902290 · 1990-08-01

Decision Date1990-08-01
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

ITE HEARING AID MODEL PALOMINO is the device name listed in this FDA 510(k) record. The listed applicant is Improved Hearing Service, Inc.. It received FDA 510(k) clearance on 1990-08-01 under 510(k) number K902290. 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 ITE HEARING AID MODEL PALOMINO?

ITE HEARING AID MODEL PALOMINO is a medical device that received FDA 510(k) clearance on 1990-08-01. The listed applicant is Improved Hearing Service, Inc.. The 510(k) number is K902290.

When did ITE HEARING AID MODEL PALOMINO receive FDA 510(k) clearance?

ITE HEARING AID MODEL PALOMINO received FDA 510(k) clearance on 1990-08-01, under 510(k) number K902290.

Who is the listed applicant for ITE HEARING AID MODEL PALOMINO?

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

What is the FDA product code for ITE HEARING AID MODEL PALOMINO?

The FDA product code for ITE HEARING AID MODEL PALOMINO 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 Improved Hearing Service, 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 9 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.

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