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FDA 510(k)

MODEL H39C-BEHING-THE-EAR HEARING INSTRU

K-Number: K790779 · 1979-05-16

Decision Date1979-05-16
Product Code
DecisionSubstantially Equivalent

Device Summary

MODEL H39C-BEHING-THE-EAR HEARING INSTRU is the device name listed in this FDA 510(k) record. The listed applicant is Marcon Hearing Instruments, Inc.. It received FDA 510(k) clearance on 1979-05-16 under 510(k) number K790779. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL H39C-BEHING-THE-EAR HEARING INSTRU?

MODEL H39C-BEHING-THE-EAR HEARING INSTRU is a medical device that received FDA 510(k) clearance on 1979-05-16. The listed applicant is Marcon Hearing Instruments, Inc.. The 510(k) number is K790779.

When did MODEL H39C-BEHING-THE-EAR HEARING INSTRU receive FDA 510(k) clearance?

MODEL H39C-BEHING-THE-EAR HEARING INSTRU received FDA 510(k) clearance on 1979-05-16, under 510(k) number K790779.

Who is the listed applicant for MODEL H39C-BEHING-THE-EAR HEARING INSTRU?

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

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 Marcon Hearing Instruments, 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.

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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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