SUPERA VERITAS
K-Number: K130591 · 2013-05-02
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Device Summary
Frequently Asked Questions
What is the SUPERA VERITAS?
SUPERA VERITAS is a medical device that received FDA 510(k) clearance on 2013-05-02. The listed applicant is Idev Technologies, Inc.. The 510(k) number is K130591.
When did SUPERA VERITAS receive FDA 510(k) clearance?
SUPERA VERITAS received FDA 510(k) clearance on 2013-05-02, under 510(k) number K130591.
Who is the listed applicant for SUPERA VERITAS?
The FDA 510(k) record lists Idev Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SUPERA VERITAS?
The FDA product code for SUPERA VERITAS is FGE.
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 Idev Technologies, 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: FGE)
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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