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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 the device name listed in this FDA 510(k) record. The listed applicant is Clarteis. It received FDA 510(k) clearance on 2017-10-13 under 510(k) 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. The listed applicant is Clarteis. The 510(k) number is K171702.

When did Exciplex308nm receive FDA 510(k) clearance?

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

Who is the listed applicant for Exciplex308nm?

The FDA 510(k) record lists Clarteis as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Exciplex308nm?

The FDA product code for Exciplex308nm is FTC.

Other records listing Clarteis 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.

Related Devices (Code: FTC)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.