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FDA 510(k)

MODEL 340 PROBE MIC SYSTEM

K-Number: K896301 · 1990-01-16

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

Device Summary

MODEL 340 PROBE MIC 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 K896301. The device is classified under product code ETW. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 340 PROBE MIC SYSTEM?

MODEL 340 PROBE MIC 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 K896301.

When did MODEL 340 PROBE MIC SYSTEM receive FDA 510(k) clearance?

MODEL 340 PROBE MIC SYSTEM received FDA 510(k) clearance on 1990-01-16, under 510(k) number K896301.

Who is the listed applicant for MODEL 340 PROBE MIC 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 340 PROBE MIC SYSTEM?

The FDA product code for MODEL 340 PROBE MIC SYSTEM is ETW.

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.

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.

View all 9 devices →

Related Devices (Code: ETW)

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.

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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