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FDA 510(k)

VISUALIZER 2000

K-Number: K943272 · 1994-12-27

ApplicantVf-Works, Inc.
Decision Date1994-12-27
Product CodeJAA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VISUALIZER 2000 is the device name listed in this FDA 510(k) record. The listed applicant is Vf-Works, Inc.. It received FDA 510(k) clearance on 1994-12-27 under 510(k) number K943272. The device is classified under product code JAA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VISUALIZER 2000?

VISUALIZER 2000 is a medical device that received FDA 510(k) clearance on 1994-12-27. The listed applicant is Vf-Works, Inc.. The 510(k) number is K943272.

When did VISUALIZER 2000 receive FDA 510(k) clearance?

VISUALIZER 2000 received FDA 510(k) clearance on 1994-12-27, under 510(k) number K943272.

Who is the listed applicant for VISUALIZER 2000?

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

What is the FDA product code for VISUALIZER 2000?

The FDA product code for VISUALIZER 2000 is JAA.

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Related Devices (Code: JAA)

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.

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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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