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)

SEARS MODEL 9098 ITE HEARING AID

K-Number: K901351 · 1990-04-27

Decision Date1990-04-27
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

SEARS MODEL 9098 ITE HEARING AID is the device name listed in this FDA 510(k) record. The listed applicant is Miracle-Ear, Inc.. It received FDA 510(k) clearance on 1990-04-27 under 510(k) number K901351. 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 SEARS MODEL 9098 ITE HEARING AID?

SEARS MODEL 9098 ITE HEARING AID is a medical device that received FDA 510(k) clearance on 1990-04-27. The listed applicant is Miracle-Ear, Inc.. The 510(k) number is K901351.

When did SEARS MODEL 9098 ITE HEARING AID receive FDA 510(k) clearance?

SEARS MODEL 9098 ITE HEARING AID received FDA 510(k) clearance on 1990-04-27, under 510(k) number K901351.

Who is the listed applicant for SEARS MODEL 9098 ITE HEARING AID?

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

What is the FDA product code for SEARS MODEL 9098 ITE HEARING AID?

The FDA product code for SEARS MODEL 9098 ITE HEARING AID 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 Miracle-Ear, 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 65 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.

↑