FDA 510(k)

DOCE ALL-IN-THE-EAR AID

K-Number: K822817 · 1983-01-18

ApplicantFidelty Hearing Instruments, Inc.

Decision Date1983-01-18

Product CodeFSD

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

DOCE ALL-IN-THE-EAR AID is the device name listed in this FDA 510(k) record. The listed applicant is Fidelty Hearing Instruments, Inc.. It received FDA 510(k) clearance on 1983-01-18 under 510(k) number K822817. The device is classified under product code FSD. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DOCE ALL-IN-THE-EAR AID?

DOCE ALL-IN-THE-EAR AID is a medical device that received FDA 510(k) clearance on 1983-01-18. The listed applicant is Fidelty Hearing Instruments, Inc.. The 510(k) number is K822817.

When did DOCE ALL-IN-THE-EAR AID receive FDA 510(k) clearance?

DOCE ALL-IN-THE-EAR AID received FDA 510(k) clearance on 1983-01-18, under 510(k) number K822817.

Who is the listed applicant for DOCE ALL-IN-THE-EAR AID?

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

What is the FDA product code for DOCE ALL-IN-THE-EAR AID?

The FDA product code for DOCE ALL-IN-THE-EAR AID is FSD.

Related Devices (Code: FSD)

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.

K892379THE POUCH GROIN & ABDOMINAL STRESS AIDKuhn Industries K810379EARETTE HEARING AID SEARS #8054Oticon Corp.K770162MATERNITY SUPPORTERR.G. Moore K760772DISPOSABLE ABDOMINAL BINDERTecnol New Jersey Wound Care, Inc.

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.