ReVISION 2
K-Number: K251417 · 2026-09-09
Device Summary
Frequently Asked Questions
What is the ReVISION 2?
ReVISION 2 is a medical device that received FDA 510(k) clearance on 2026-09-09. The listed applicant is Argus Cognitive, Inc.. The 510(k) number is K251417.
When did ReVISION 2 receive FDA 510(k) clearance?
ReVISION 2 received FDA 510(k) clearance on 2026-09-09, under 510(k) number K251417.
Who is the listed applicant for ReVISION 2?
The FDA 510(k) record lists Argus Cognitive, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ReVISION 2?
The FDA product code for ReVISION 2 is QIH.
Other records listing Argus Cognitive, 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: QIH)
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.