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FDA 510(k)

MODEL 222 CLINICAL AUDIOMETER

K-Number: K934715 · 1994-05-10

ApplicantVirtual Corp.
Decision Date1994-05-10
Product CodeEWO
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

MODEL 222 CLINICAL AUDIOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Virtual Corp.. It received FDA 510(k) clearance on 1994-05-10 under 510(k) number K934715. 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 MODEL 222 CLINICAL AUDIOMETER?

MODEL 222 CLINICAL AUDIOMETER is a medical device that received FDA 510(k) clearance on 1994-05-10. The listed applicant is Virtual Corp.. The 510(k) number is K934715.

When did MODEL 222 CLINICAL AUDIOMETER receive FDA 510(k) clearance?

MODEL 222 CLINICAL AUDIOMETER received FDA 510(k) clearance on 1994-05-10, under 510(k) number K934715.

Who is the listed applicant for MODEL 222 CLINICAL AUDIOMETER?

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

What is the FDA product code for MODEL 222 CLINICAL AUDIOMETER?

The FDA product code for MODEL 222 CLINICAL AUDIOMETER is EWO.

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Other records listing Virtual Corp. 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.

K960500THE VIRTUAL M-332K930203MODEL 322 CLINICAL AUDIOMETERK926574MODEL 330 SCREENING AUDIO METER, MODIFIEDK911689MODEL 330 SCREENING AUDIOMETERK896301MODEL 340 PROBE MIC SYSTEMK895443MODEL 210 IMPEDANCE SYSTEM

View all 9 devices →

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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