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FDA 510(k)

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 the device name listed in this FDA 510(k) record. The listed applicant is C. Light Technologies, Inc.. It received FDA 510(k) clearance on 2023-05-09 under 510(k) 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. The listed applicant is C. Light Technologies, Inc.. The 510(k) number is K222484.

When did Retitrack receive FDA 510(k) clearance?

Retitrack received FDA 510(k) clearance on 2023-05-09, under 510(k) number K222484.

Who is the listed applicant for Retitrack?

The FDA 510(k) record lists C. Light Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Retitrack?

The FDA product code for Retitrack is HLL.

Related Devices (Code: HLL)

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.

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Official Source

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