Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Contour Light CL-100

K-Number: K202955 · 2021-05-19

Decision Date2021-05-19
Product CodeOLI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Contour Light CL-100 is a medical device manufactured by Contour Research, LLC. It received FDA 510(k) clearance on 2021-05-19 under approval number K202955. The device is classified under product code OLI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Contour Light CL-100?

Contour Light CL-100 is a medical device that received FDA 510(k) clearance on 2021-05-19. It is manufactured by Contour Research, LLC. The 510(k) number is K202955.

When was Contour Light CL-100 approved by the FDA?

Contour Light CL-100 received FDA 510(k) clearance on 2021-05-19, under approval number K202955.

What company makes Contour Light CL-100?

Contour Light CL-100 is manufactured by Contour Research, LLC.

What is the FDA product code for Contour Light CL-100?

The FDA product code for Contour Light CL-100 is OLI.

Other Devices by Contour Research, LLC

Related Devices (Code: OLI)

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.