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FDA 510(k)

MULTIFOCUS COMPACT BTE HEARING AID

K-Number: K933307 · 1993-08-23

ApplicantOticon, Inc.
Decision Date1993-08-23
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

MULTIFOCUS COMPACT BTE HEARING AID is the device name listed in this FDA 510(k) record. The listed applicant is Oticon, Inc.. It received FDA 510(k) clearance on 1993-08-23 under 510(k) number K933307. 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 MULTIFOCUS COMPACT BTE HEARING AID?

MULTIFOCUS COMPACT BTE HEARING AID is a medical device that received FDA 510(k) clearance on 1993-08-23. The listed applicant is Oticon, Inc.. The 510(k) number is K933307.

When did MULTIFOCUS COMPACT BTE HEARING AID receive FDA 510(k) clearance?

MULTIFOCUS COMPACT BTE HEARING AID received FDA 510(k) clearance on 1993-08-23, under 510(k) number K933307.

Who is the listed applicant for MULTIFOCUS COMPACT BTE HEARING AID?

The FDA 510(k) record lists Oticon, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MULTIFOCUS COMPACT BTE HEARING AID?

The FDA product code for MULTIFOCUS COMPACT BTE 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 Oticon, 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 9 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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