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FDA 510(k)

OTICON MF

K-Number: K932670 · 1993-08-05

ApplicantOticon Corp.
Decision Date1993-08-05
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

OTICON MF is the device name listed in this FDA 510(k) record. The listed applicant is Oticon Corp.. It received FDA 510(k) clearance on 1993-08-05 under 510(k) number K932670. 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 OTICON MF?

OTICON MF is a medical device that received FDA 510(k) clearance on 1993-08-05. The listed applicant is Oticon Corp.. The 510(k) number is K932670.

When did OTICON MF receive FDA 510(k) clearance?

OTICON MF received FDA 510(k) clearance on 1993-08-05, under 510(k) number K932670.

Who is the listed applicant for OTICON MF?

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

What is the FDA product code for OTICON MF?

The FDA product code for OTICON MF 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 Corp. 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 57 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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