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FDA 510(k)

BEHIND-THE-EAR HEARING AID MODEL 404 PP-PC

K-Number: K891247 · 1989-03-29

ApplicantSiemens Hearing Instruments, Inc.
Decision Date1989-03-29
Product CodeESF
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BEHIND-THE-EAR HEARING AID MODEL 404 PP-PC is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Hearing Instruments, Inc.. It received FDA 510(k) clearance on 1989-03-29 under 510(k) number K891247. The device is classified under product code ESF. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BEHIND-THE-EAR HEARING AID MODEL 404 PP-PC?

BEHIND-THE-EAR HEARING AID MODEL 404 PP-PC is a medical device that received FDA 510(k) clearance on 1989-03-29. The listed applicant is Siemens Hearing Instruments, Inc.. The 510(k) number is K891247.

When did BEHIND-THE-EAR HEARING AID MODEL 404 PP-PC receive FDA 510(k) clearance?

BEHIND-THE-EAR HEARING AID MODEL 404 PP-PC received FDA 510(k) clearance on 1989-03-29, under 510(k) number K891247.

Who is the listed applicant for BEHIND-THE-EAR HEARING AID MODEL 404 PP-PC?

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

What is the FDA product code for BEHIND-THE-EAR HEARING AID MODEL 404 PP-PC?

The FDA product code for BEHIND-THE-EAR HEARING AID MODEL 404 PP-PC is ESF.

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Other records listing Siemens 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.

K071462UNITY 2 HIA & PROBE ( FOR USE WITH UNITY 2)K011364CUSTOM TCI (TINNITUS CONTROL INSTRUMENT)K011366CUSTOM TCI-COMBI (TINNITUS CONTROL INSTRUMENT COMBINATION)K003559TCI (TINNITUS CONTROL INSTRUMENT)K003558TCI COMBI (TINNITUS CONTROL INSTRUMENT COMBINATION)K972998PRISMA

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Related Devices (Code: ESF)

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.

K813224CERAVITAL CERAMIC EAR CANAL WALL PROSTHXomed, Inc.

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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