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FDA 510(k)

MODEL 330 SCREENING AUDIO METER, MODIFIED

K-Number: K926574 · 1993-03-29

ApplicantVirtual Corp.
Decision Date1993-03-29
Product CodeGWJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MODEL 330 SCREENING AUDIO METER, MODIFIED is the device name listed in this FDA 510(k) record. The listed applicant is Virtual Corp.. It received FDA 510(k) clearance on 1993-03-29 under 510(k) number K926574. The device is classified under product code GWJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 330 SCREENING AUDIO METER, MODIFIED?

MODEL 330 SCREENING AUDIO METER, MODIFIED is a medical device that received FDA 510(k) clearance on 1993-03-29. The listed applicant is Virtual Corp.. The 510(k) number is K926574.

When did MODEL 330 SCREENING AUDIO METER, MODIFIED receive FDA 510(k) clearance?

MODEL 330 SCREENING AUDIO METER, MODIFIED received FDA 510(k) clearance on 1993-03-29, under 510(k) number K926574.

Who is the listed applicant for MODEL 330 SCREENING AUDIO METER, MODIFIED?

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 330 SCREENING AUDIO METER, MODIFIED?

The FDA product code for MODEL 330 SCREENING AUDIO METER, MODIFIED is GWJ.

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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-332K934715MODEL 222 CLINICAL AUDIOMETERK930203MODEL 322 CLINICAL AUDIOMETERK911689MODEL 330 SCREENING AUDIOMETERK896301MODEL 340 PROBE MIC SYSTEMK895443MODEL 210 IMPEDANCE SYSTEM

View all 9 devices →

Related Devices (Code: GWJ)

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.

K242954Integrity V500 (Integrity, Integrity with VEMP)Vivosonic, Inc.K233649ALGO Pro Newborn Hearing Screener (ALGO Pro)Natus Medical Incorporated Dba Excel-Tech Ltd. (Xltek)K220139QScreenPath Medical GmbHK211147ALGO 7iPath Medical GmbHK193033GSI Audera ProGrason StadlerK163326SmartEPIntelligent Hearing Systems

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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