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FDA 510(k)

HEARING AID M35/M36 SERIES

K-Number: K872556 · 1987-07-16

Decision Date1987-07-16
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

HEARING AID M35/M36 SERIES is the device name listed in this FDA 510(k) record. The listed applicant is Electone, Inc.. It received FDA 510(k) clearance on 1987-07-16 under 510(k) number K872556. 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 HEARING AID M35/M36 SERIES?

HEARING AID M35/M36 SERIES is a medical device that received FDA 510(k) clearance on 1987-07-16. The listed applicant is Electone, Inc.. The 510(k) number is K872556.

When did HEARING AID M35/M36 SERIES receive FDA 510(k) clearance?

HEARING AID M35/M36 SERIES received FDA 510(k) clearance on 1987-07-16, under 510(k) number K872556.

Who is the listed applicant for HEARING AID M35/M36 SERIES?

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

What is the FDA product code for HEARING AID M35/M36 SERIES?

The FDA product code for HEARING AID M35/M36 SERIES 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 Electone, 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 73 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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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