BESTONE MODEL ITE & CANAL
K-Number: K893887 · 1990-01-23
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Device Summary
Frequently Asked Questions
What is the BESTONE MODEL ITE & CANAL?
BESTONE MODEL ITE & CANAL is a medical device that received FDA 510(k) clearance on 1990-01-23. The listed applicant is Bestone Hearing Instruments. The 510(k) number is K893887.
When did BESTONE MODEL ITE & CANAL receive FDA 510(k) clearance?
BESTONE MODEL ITE & CANAL received FDA 510(k) clearance on 1990-01-23, under 510(k) number K893887.
Who is the listed applicant for BESTONE MODEL ITE & CANAL?
The FDA 510(k) record lists Bestone Hearing Instruments as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BESTONE MODEL ITE & CANAL?
The FDA product code for BESTONE MODEL ITE & CANAL 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.
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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