NOMAD DENTAL X-RAY SYSTEM
K-Number: K051795 · 2005-07-14
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Device Summary
Frequently Asked Questions
What is the NOMAD DENTAL X-RAY SYSTEM?
NOMAD DENTAL X-RAY SYSTEM is a medical device that received FDA 510(k) clearance on 2005-07-14. The listed applicant is Aribex, Inc.. The 510(k) number is K051795.
When did NOMAD DENTAL X-RAY SYSTEM receive FDA 510(k) clearance?
NOMAD DENTAL X-RAY SYSTEM received FDA 510(k) clearance on 2005-07-14, under 510(k) number K051795.
Who is the listed applicant for NOMAD DENTAL X-RAY SYSTEM?
The FDA 510(k) record lists Aribex, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NOMAD DENTAL X-RAY SYSTEM?
The FDA product code for NOMAD DENTAL X-RAY SYSTEM is EHD.
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 Aribex, Inc. 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: EHD)
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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