CENTRAL VISION ANALYZER MODEL 1000
K-Number: K100095 · 2010-05-10
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Device Summary
Frequently Asked Questions
What is the CENTRAL VISION ANALYZER MODEL 1000?
CENTRAL VISION ANALYZER MODEL 1000 is a medical device that received FDA 510(k) clearance on 2010-05-10. The listed applicant is Vimetrics,Llc.. The 510(k) number is K100095.
When did CENTRAL VISION ANALYZER MODEL 1000 receive FDA 510(k) clearance?
CENTRAL VISION ANALYZER MODEL 1000 received FDA 510(k) clearance on 2010-05-10, under 510(k) number K100095.
Who is the listed applicant for CENTRAL VISION ANALYZER MODEL 1000?
The FDA 510(k) record lists Vimetrics,Llc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CENTRAL VISION ANALYZER MODEL 1000?
The FDA product code for CENTRAL VISION ANALYZER MODEL 1000 is HOX.
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.
Related Devices (Code: HOX)
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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