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FDA 510(k)

AMPLAID 171S

K-Number: K972862 · 1997-10-31

ApplicantAmplifon S.P.A.
Decision Date1997-10-31
Product CodeEWO
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

AMPLAID 171S is the device name listed in this FDA 510(k) record. The listed applicant is Amplifon S.P.A.. It received FDA 510(k) clearance on 1997-10-31 under 510(k) number K972862. The device is classified under product code EWO. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMPLAID 171S?

AMPLAID 171S is a medical device that received FDA 510(k) clearance on 1997-10-31. The listed applicant is Amplifon S.P.A.. The 510(k) number is K972862.

When did AMPLAID 171S receive FDA 510(k) clearance?

AMPLAID 171S received FDA 510(k) clearance on 1997-10-31, under 510(k) number K972862.

Who is the listed applicant for AMPLAID 171S?

The FDA 510(k) record lists Amplifon S.P.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AMPLAID 171S?

The FDA product code for AMPLAID 171S is EWO.

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.

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Other records listing Amplifon S.P.A. 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.

K992370AMPLAID A724 AND A728K983915AMPLAID A315 AND A319K983712AMPLAID A311 SERIESK971740AMPLAID MK12K974235AMPLAID AM50K972959AMPLAID MK22

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Related Devices (Code: EWO)

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.

K234095OtoNova/OtoNova ProOtodynamicsK240430Otoport ProOtodynamics, Ltd.K231545hearOAEHearx SA (Pty) , Ltd.K213345Sentiero, AuDX, AuDX PRO, Sentiero Desktop, AuDX PRO Flex, Sentiero Advanced, NavPRO ONEPath Medical GmbHK191372LyraInteracoustics A/SK180287GSI CortiGrason-Stadler, 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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