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FDA 510(k)

Exciplex308nm

K-Number: K171702 · 2017-10-13

ApplicantClarteis
Decision Date2017-10-13
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Exciplex308nm is a medical device manufactured by Clarteis. It received FDA 510(k) clearance on 2017-10-13 under approval number K171702. The device is classified under product code FTC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Exciplex308nm?

Exciplex308nm is a medical device that received FDA 510(k) clearance on 2017-10-13. It is manufactured by Clarteis. The 510(k) number is K171702.

When was Exciplex308nm approved by the FDA?

Exciplex308nm received FDA 510(k) clearance on 2017-10-13, under approval number K171702.

What company makes Exciplex308nm?

Exciplex308nm is manufactured by Clarteis.

What is the FDA product code for Exciplex308nm?

The FDA product code for Exciplex308nm is FTC.

Other Devices by Clarteis

K191086Exciplex

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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.

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