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FDA 510(k)

VOXAR'S CALCIUM SCORING PRODUCT

K-Number: K020140 · 2002-01-28

ApplicantVoxar Limited
Decision Date2002-01-28
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VOXAR'S CALCIUM SCORING PRODUCT is the device name listed in this FDA 510(k) record. The listed applicant is Voxar Limited. It received FDA 510(k) clearance on 2002-01-28 under 510(k) number K020140. 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'S CALCIUM SCORING PRODUCT?

VOXAR'S CALCIUM SCORING PRODUCT is a medical device that received FDA 510(k) clearance on 2002-01-28. The listed applicant is Voxar Limited. The 510(k) number is K020140.

When did VOXAR'S CALCIUM SCORING PRODUCT receive FDA 510(k) clearance?

VOXAR'S CALCIUM SCORING PRODUCT received FDA 510(k) clearance on 2002-01-28, under 510(k) number K020140.

Who is the listed applicant for VOXAR'S CALCIUM SCORING PRODUCT?

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'S CALCIUM SCORING PRODUCT?

The FDA product code for VOXAR'S CALCIUM SCORING PRODUCT 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.

K043194VOXAR 3D PRODUCT FAMILYK012072VOXAR VC, MODEL 1.0K992654PLUG 'N VIEW 3D, VERSION 1.0

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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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