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FDA 510(k)

BESTONE MODEL ITE & CANAL

K-Number: K893887 · 1990-01-23

Decision Date1990-01-23
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

BESTONE MODEL ITE & CANAL is the device name listed in this FDA 510(k) record. The listed applicant is Bestone Hearing Instruments. It received FDA 510(k) clearance on 1990-01-23 under 510(k) number K893887. 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 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

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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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