VISIOFOCUS
K-Number: K122412 · 2013-03-13
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Device Summary
Frequently Asked Questions
What is the VISIOFOCUS?
VISIOFOCUS is a medical device that received FDA 510(k) clearance on 2013-03-13. The listed applicant is Tecnimed S.R.L.. The 510(k) number is K122412.
When did VISIOFOCUS receive FDA 510(k) clearance?
VISIOFOCUS received FDA 510(k) clearance on 2013-03-13, under 510(k) number K122412.
Who is the listed applicant for VISIOFOCUS?
The FDA 510(k) record lists Tecnimed S.R.L. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VISIOFOCUS?
The FDA product code for VISIOFOCUS is FLL.
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 Tecnimed S.R.L. 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: FLL)
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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