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FDA 510(k)

VOXAR 3D PRODUCT FAMILY

K-Number: K043194 · 2005-01-11

ApplicantVoxar Limited
Decision Date2005-01-11
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VOXAR 3D PRODUCT FAMILY is the device name listed in this FDA 510(k) record. The listed applicant is Voxar Limited. It received FDA 510(k) clearance on 2005-01-11 under 510(k) number K043194. 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 VOXAR 3D PRODUCT FAMILY?

VOXAR 3D PRODUCT FAMILY is a medical device that received FDA 510(k) clearance on 2005-01-11. The listed applicant is Voxar Limited. The 510(k) number is K043194.

When did VOXAR 3D PRODUCT FAMILY receive FDA 510(k) clearance?

VOXAR 3D PRODUCT FAMILY received FDA 510(k) clearance on 2005-01-11, under 510(k) number K043194.

Who is the listed applicant for VOXAR 3D PRODUCT FAMILY?

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 VOXAR 3D PRODUCT FAMILY?

The FDA product code for VOXAR 3D PRODUCT FAMILY is LLZ.

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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.

K020140VOXAR'S CALCIUM SCORING PRODUCTK012072VOXAR VC, MODEL 1.0K992654PLUG 'N VIEW 3D, VERSION 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.

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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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