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FDA 510(k)

RELINER FOR HEARING AID EARMOLDS

K-Number: K820185 · 1982-04-09

Decision Date1982-04-09
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

RELINER FOR HEARING AID EARMOLDS is the device name listed in this FDA 510(k) record. The listed applicant is Aid-To-Hearing Corp.. It received FDA 510(k) clearance on 1982-04-09 under 510(k) number K820185. 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 RELINER FOR HEARING AID EARMOLDS?

RELINER FOR HEARING AID EARMOLDS is a medical device that received FDA 510(k) clearance on 1982-04-09. The listed applicant is Aid-To-Hearing Corp.. The 510(k) number is K820185.

When did RELINER FOR HEARING AID EARMOLDS receive FDA 510(k) clearance?

RELINER FOR HEARING AID EARMOLDS received FDA 510(k) clearance on 1982-04-09, under 510(k) number K820185.

Who is the listed applicant for RELINER FOR HEARING AID EARMOLDS?

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

What is the FDA product code for RELINER FOR HEARING AID EARMOLDS?

The FDA product code for RELINER FOR HEARING AID EARMOLDS 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.

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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