VOXAR 3D ENTERPRISE, MODEL 6.1
K-Number: K060505 · 2006-03-29
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Device Summary
Frequently Asked Questions
What is the VOXAR 3D ENTERPRISE, MODEL 6.1?
VOXAR 3D ENTERPRISE, MODEL 6.1 is a medical device that received FDA 510(k) clearance on 2006-03-29. The listed applicant is Barcoview Mis Edinburgh. The 510(k) number is K060505.
When did VOXAR 3D ENTERPRISE, MODEL 6.1 receive FDA 510(k) clearance?
VOXAR 3D ENTERPRISE, MODEL 6.1 received FDA 510(k) clearance on 2006-03-29, under 510(k) number K060505.
Who is the listed applicant for VOXAR 3D ENTERPRISE, MODEL 6.1?
The FDA 510(k) record lists Barcoview Mis Edinburgh as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VOXAR 3D ENTERPRISE, MODEL 6.1?
The FDA product code for VOXAR 3D ENTERPRISE, MODEL 6.1 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.
Other records listing Barcoview Mis Edinburgh 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.
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.
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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