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FDA 510(k)

MODEL 210 IMPEDANCE SYSTEM

K-Number: K895443 · 1990-01-16

ApplicantVirtual Corp.
Decision Date1990-01-16
Product CodeETY
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

MODEL 210 IMPEDANCE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Virtual Corp.. It received FDA 510(k) clearance on 1990-01-16 under 510(k) number K895443. The device is classified under product code ETY. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 210 IMPEDANCE SYSTEM?

MODEL 210 IMPEDANCE SYSTEM is a medical device that received FDA 510(k) clearance on 1990-01-16. The listed applicant is Virtual Corp.. The 510(k) number is K895443.

When did MODEL 210 IMPEDANCE SYSTEM receive FDA 510(k) clearance?

MODEL 210 IMPEDANCE SYSTEM received FDA 510(k) clearance on 1990-01-16, under 510(k) number K895443.

Who is the listed applicant for MODEL 210 IMPEDANCE SYSTEM?

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 210 IMPEDANCE SYSTEM?

The FDA product code for MODEL 210 IMPEDANCE SYSTEM is ETY.

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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 AUDIOMETERK926574MODEL 330 SCREENING AUDIO METER, MODIFIEDK911689MODEL 330 SCREENING AUDIOMETERK896301MODEL 340 PROBE MIC SYSTEM

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Related Devices (Code: ETY)

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.

K183201Hearing Healthcare ProDb Diagnostic Systems, Inc.K171038Hearing Healthcare ProDb Diagnostic Systems, Inc.K162210touchTympMaico Diagnostics GmbHK161707Madsen ZodiacGn OtometricsK121847TITANInteracoustics A/SK083861TITAN, TITAN SHOULDER BOX, TITAN CRADLE, TITAN PRINTER, TITAN IMP440, IMP440 MODULE, TITAN SUITEInteracoustics AS

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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