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FDA 510(k)

VIRTUAL MEDICAL SYSTEMS MODEL VT3000

K-Number: K052904 · 2005-10-27

Decision Date2005-10-27
Product CodeJXE
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

VIRTUAL MEDICAL SYSTEMS MODEL VT3000 is the device name listed in this FDA 510(k) record. The listed applicant is Scientific Imaging, Inc.. It received FDA 510(k) clearance on 2005-10-27 under 510(k) number K052904. The device is classified under product code JXE. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIRTUAL MEDICAL SYSTEMS MODEL VT3000?

VIRTUAL MEDICAL SYSTEMS MODEL VT3000 is a medical device that received FDA 510(k) clearance on 2005-10-27. The listed applicant is Scientific Imaging, Inc.. The 510(k) number is K052904.

When did VIRTUAL MEDICAL SYSTEMS MODEL VT3000 receive FDA 510(k) clearance?

VIRTUAL MEDICAL SYSTEMS MODEL VT3000 received FDA 510(k) clearance on 2005-10-27, under 510(k) number K052904.

Who is the listed applicant for VIRTUAL MEDICAL SYSTEMS MODEL VT3000?

The FDA 510(k) record lists Scientific Imaging, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VIRTUAL MEDICAL SYSTEMS MODEL VT3000?

The FDA product code for VIRTUAL MEDICAL SYSTEMS MODEL VT3000 is JXE.

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 Scientific Imaging, Inc. 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.

Related Devices (Code: JXE)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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