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FDA 510(k)

ClearCheck Model RADCC V2

K-Number: K220583 · 2022-08-23

Decision Date2022-08-23
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ClearCheck Model RADCC V2 is the device name listed in this FDA 510(k) record. The listed applicant is Radformation, Inc.. It received FDA 510(k) clearance on 2022-08-23 under 510(k) 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. 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.

View all 16 devices →

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.