Retitrack
K-Number: K222484 · 2023-05-09
ApplicantC. Light Technologies, Inc.
Decision Date2023-05-09
Product CodeHLL
Advisory CommitteeOP
DecisionSubstantially Equivalent
Device Summary
Retitrack is a medical device manufactured by C. Light Technologies, Inc.. It received FDA 510(k) clearance on 2023-05-09 under approval number K222484. The device is classified under product code HLL. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Retitrack?
Retitrack is a medical device that received FDA 510(k) clearance on 2023-05-09. It is manufactured by C. Light Technologies, Inc.. The 510(k) number is K222484.
When was Retitrack approved by the FDA?
Retitrack received FDA 510(k) clearance on 2023-05-09, under approval number K222484.
What company makes Retitrack?
Retitrack is manufactured by C. Light Technologies, Inc..
What is the FDA product code for Retitrack?
The FDA product code for Retitrack is HLL.
Related Devices (Code: HLL)
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.