MULTI-CHANNEL COMPRESSION BTE (SD)
K-Number: K970262 · 1997-03-31
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Device Summary
Frequently Asked Questions
What is the MULTI-CHANNEL COMPRESSION BTE (SD)?
MULTI-CHANNEL COMPRESSION BTE (SD) is a medical device that received FDA 510(k) clearance on 1997-03-31. The listed applicant is Miracle-Ear, Inc.. The 510(k) number is K970262.
When did MULTI-CHANNEL COMPRESSION BTE (SD) receive FDA 510(k) clearance?
MULTI-CHANNEL COMPRESSION BTE (SD) received FDA 510(k) clearance on 1997-03-31, under 510(k) number K970262.
Who is the listed applicant for MULTI-CHANNEL COMPRESSION BTE (SD)?
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 MULTI-CHANNEL COMPRESSION BTE (SD)?
The FDA product code for MULTI-CHANNEL COMPRESSION BTE (SD) 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.
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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