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FDA 510(k)

ITE HEARING AID, EAR-TRONICS MODELS: M1-M23

K-Number: K881299 · 1988-08-05

Decision Date1988-08-05
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

ITE HEARING AID, EAR-TRONICS MODELS: M1-M23 is the device name listed in this FDA 510(k) record. The listed applicant is Ear-Tronics, Inc.. It received FDA 510(k) clearance on 1988-08-05 under 510(k) number K881299. 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, EAR-TRONICS MODELS: M1-M23?

ITE HEARING AID, EAR-TRONICS MODELS: M1-M23 is a medical device that received FDA 510(k) clearance on 1988-08-05. The listed applicant is Ear-Tronics, Inc.. The 510(k) number is K881299.

When did ITE HEARING AID, EAR-TRONICS MODELS: M1-M23 receive FDA 510(k) clearance?

ITE HEARING AID, EAR-TRONICS MODELS: M1-M23 received FDA 510(k) clearance on 1988-08-05, under 510(k) number K881299.

Who is the listed applicant for ITE HEARING AID, EAR-TRONICS MODELS: M1-M23?

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

What is the FDA product code for ITE HEARING AID, EAR-TRONICS MODELS: M1-M23?

The FDA product code for ITE HEARING AID, EAR-TRONICS MODELS: M1-M23 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 Ear-Tronics, 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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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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