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FDA 510(k)

THE VIRTUAL M-332

K-Number: K960500 · 1996-04-03

ApplicantVirtual Corp.
Decision Date1996-04-03
Product CodeEWD
DecisionSubstantially Equivalent

Device Summary

THE VIRTUAL M-332 is the device name listed in this FDA 510(k) record. The listed applicant is Virtual Corp.. It received FDA 510(k) clearance on 1996-04-03 under 510(k) number K960500. The device is classified under product code EWD. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE VIRTUAL M-332?

THE VIRTUAL M-332 is a medical device that received FDA 510(k) clearance on 1996-04-03. The listed applicant is Virtual Corp.. The 510(k) number is K960500.

When did THE VIRTUAL M-332 receive FDA 510(k) clearance?

THE VIRTUAL M-332 received FDA 510(k) clearance on 1996-04-03, under 510(k) number K960500.

Who is the listed applicant for THE VIRTUAL M-332?

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 THE VIRTUAL M-332?

The FDA product code for THE VIRTUAL M-332 is EWD.

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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.

K934715MODEL 222 CLINICAL AUDIOMETERK930203MODEL 322 CLINICAL AUDIOMETERK926574MODEL 330 SCREENING AUDIO METER, MODIFIEDK911689MODEL 330 SCREENING AUDIOMETERK896301MODEL 340 PROBE MIC SYSTEMK895443MODEL 210 IMPEDANCE SYSTEM

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Related Devices (Code: EWD)

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.

K020296ADULT SILICONE EAR PLUGS, MODELS # 68053, 68057Apothecary Products, Inc.K972923SUPER SILIPLUGS EAR PLUGSInterview Medical Technology Corp.K971517SILICONE PUTTY EAR PLUGSBentec Medical, Inc.K962292HEARSAVEREmtech LaboratoriesK945376DOC'S PROPLUGS EAR PLUGSDoc'S Proplugs, Inc.K930203MODEL 322 CLINICAL AUDIOMETERVirtual Corp.

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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