ClearCheck Model RADCC V2
K-Number: K220583 · 2022-08-23
Device Summary
Frequently Asked Questions
What is the ClearCheck Model RADCC V2?
ClearCheck Model RADCC V2 is a medical device that received FDA 510(k) clearance on 2022-08-23. The listed applicant is Radformation, Inc.. The 510(k) number is K220583.
When did ClearCheck Model RADCC V2 receive FDA 510(k) clearance?
ClearCheck Model RADCC V2 received FDA 510(k) clearance on 2022-08-23, under 510(k) number K220583.
Who is the listed applicant for ClearCheck Model RADCC V2?
The FDA 510(k) record lists Radformation, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ClearCheck Model RADCC V2?
The FDA product code for ClearCheck Model RADCC V2 is IYE.
Other records listing Radformation, 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: IYE)
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.