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FDA 510(k)

PLUG 'N VIEW 3D, VERSION 1.0

K-Number: K992654 · 1999-11-05

ApplicantVoxar Limited
Decision Date1999-11-05
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PLUG 'N VIEW 3D, VERSION 1.0 is the device name listed in this FDA 510(k) record. The listed applicant is Voxar Limited. It received FDA 510(k) clearance on 1999-11-05 under 510(k) number K992654. 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 PLUG 'N VIEW 3D, VERSION 1.0?

PLUG 'N VIEW 3D, VERSION 1.0 is a medical device that received FDA 510(k) clearance on 1999-11-05. The listed applicant is Voxar Limited. The 510(k) number is K992654.

When did PLUG 'N VIEW 3D, VERSION 1.0 receive FDA 510(k) clearance?

PLUG 'N VIEW 3D, VERSION 1.0 received FDA 510(k) clearance on 1999-11-05, under 510(k) number K992654.

Who is the listed applicant for PLUG 'N VIEW 3D, VERSION 1.0?

The FDA 510(k) record lists Voxar Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PLUG 'N VIEW 3D, VERSION 1.0?

The FDA product code for PLUG 'N VIEW 3D, VERSION 1.0 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 Voxar Limited 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.

K043194VOXAR 3D PRODUCT FAMILYK020140VOXAR'S CALCIUM SCORING PRODUCTK012072VOXAR VC, MODEL 1.0

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

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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