ITE HEARING AID, EAR-TRONICS MODELS: M1-M23
K-Number: K881299 · 1988-08-05
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Device Summary
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
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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