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FDA 510(k)

VIZDEXTER VERSION 2.0; DEXTROSCOPE MK8; DEXTROBEAM MK3

K-Number: K022938 · 2002-10-25

ApplicantVolume Interactions Pte, Ltd.
Decision Date2002-10-25
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VIZDEXTER VERSION 2.0; DEXTROSCOPE MK8; DEXTROBEAM MK3 is the device name listed in this FDA 510(k) record. The listed applicant is Volume Interactions Pte, Ltd.. It received FDA 510(k) clearance on 2002-10-25 under 510(k) number K022938. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIZDEXTER VERSION 2.0; DEXTROSCOPE MK8; DEXTROBEAM MK3?

VIZDEXTER VERSION 2.0; DEXTROSCOPE MK8; DEXTROBEAM MK3 is a medical device that received FDA 510(k) clearance on 2002-10-25. The listed applicant is Volume Interactions Pte, Ltd.. The 510(k) number is K022938.

When did VIZDEXTER VERSION 2.0; DEXTROSCOPE MK8; DEXTROBEAM MK3 receive FDA 510(k) clearance?

VIZDEXTER VERSION 2.0; DEXTROSCOPE MK8; DEXTROBEAM MK3 received FDA 510(k) clearance on 2002-10-25, under 510(k) number K022938.

Who is the listed applicant for VIZDEXTER VERSION 2.0; DEXTROSCOPE MK8; DEXTROBEAM MK3?

The FDA 510(k) record lists Volume Interactions Pte, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VIZDEXTER VERSION 2.0; DEXTROSCOPE MK8; DEXTROBEAM MK3?

The FDA product code for VIZDEXTER VERSION 2.0; DEXTROSCOPE MK8; DEXTROBEAM MK3 is LLZ.

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.

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Other records listing Volume Interactions Pte, Ltd. 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.

K071054RADIODEXTER, DEXTROSCOPE, DEXTROBEAM, MODELS 1.0, MK10, MK3 & MK4K063730DEXTROSCOPE, MODEL MK10; DEXTROBEAM, MODEL MK3, MK4; RADIODEXTER, MODEL 1.0K053162DEXTROSCOPE & DEXTROBEAMK032924RADIODEXTER VERSION 1.0, DEXTROSCOPE, MODEL MK10 AND DEXTROBEAM, MODEL MK3

Related Devices (Code: LLZ)

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.

K261874Syneris PACS v.1.0.1.0SynerisK262442HipStudio AnalysisReplasia BVK261855Elucid PlaqueIQElucid Bioimaging, Inc.K254214OOOPDSTaiwan Main Orthopaedic Biotechnology Co., Ltd.K261861SPINEsim v1.0Mdsim S.A.K2620603D-RD-SRadiopharmaceutical Imaging & Dosimetry, LLC

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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