ClearCheck Model RADCC V2
K-Number: K220583 · 2022-08-23
ApplicantRadformation, Inc.
Decision Date2022-08-23
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
ClearCheck Model RADCC V2 is a medical device manufactured by Radformation, Inc.. It received FDA 510(k) clearance on 2022-08-23 under approval number K220583. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
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. It is manufactured by Radformation, Inc.. The 510(k) number is K220583.
When was ClearCheck Model RADCC V2 approved by the FDA?
ClearCheck Model RADCC V2 received FDA 510(k) clearance on 2022-08-23, under approval number K220583.
What company makes ClearCheck Model RADCC V2?
ClearCheck Model RADCC V2 is manufactured by Radformation, Inc..
What is the FDA product code for ClearCheck Model RADCC V2?
The FDA product code for ClearCheck Model RADCC V2 is IYE.
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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.