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FDA 510(k)

INTERNATIONAL MODEL SC CANAL IN THE EAR HEARING AI

K-Number: K853172 · 1985-10-17

Decision Date1985-10-17
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

INTERNATIONAL MODEL SC CANAL IN THE EAR HEARING AI is the device name listed in this FDA 510(k) record. The listed applicant is Int'L Hearing Aids, Inc.. It received FDA 510(k) clearance on 1985-10-17 under 510(k) number K853172. 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 INTERNATIONAL MODEL SC CANAL IN THE EAR HEARING AI?

INTERNATIONAL MODEL SC CANAL IN THE EAR HEARING AI is a medical device that received FDA 510(k) clearance on 1985-10-17. The listed applicant is Int'L Hearing Aids, Inc.. The 510(k) number is K853172.

When did INTERNATIONAL MODEL SC CANAL IN THE EAR HEARING AI receive FDA 510(k) clearance?

INTERNATIONAL MODEL SC CANAL IN THE EAR HEARING AI received FDA 510(k) clearance on 1985-10-17, under 510(k) number K853172.

Who is the listed applicant for INTERNATIONAL MODEL SC CANAL IN THE EAR HEARING AI?

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 INTERNATIONAL MODEL SC CANAL IN THE EAR HEARING AI?

The FDA product code for INTERNATIONAL MODEL SC CANAL IN THE EAR HEARING AI 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.

View all 21 devices →

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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