SEARS BEHIND-THE-EAR HEARING AID
K-Number: K800113 · 1980-02-11
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Device Summary
Frequently Asked Questions
What is the SEARS BEHIND-THE-EAR HEARING AID?
SEARS BEHIND-THE-EAR HEARING AID is a medical device that received FDA 510(k) clearance on 1980-02-11. The listed applicant is Int'L Hearing Aids, Inc.. The 510(k) number is K800113.
When did SEARS BEHIND-THE-EAR HEARING AID receive FDA 510(k) clearance?
SEARS BEHIND-THE-EAR HEARING AID received FDA 510(k) clearance on 1980-02-11, under 510(k) number K800113.
Who is the listed applicant for SEARS BEHIND-THE-EAR HEARING AID?
The FDA 510(k) record lists Int'L Hearing Aids, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SEARS BEHIND-THE-EAR HEARING AID?
The FDA product code for SEARS BEHIND-THE-EAR 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 Int'L Hearing Aids, 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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