FDA 510(k)

Kiierr 272 Laser, Kiierr 148 Laser

K-Number: K181878 · 2018-09-05

Decision Date2018-09-05

Product CodeOAP

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

Kiierr 272 Laser, Kiierr 148 Laser is a medical device manufactured by Kiierr International, LLC. It received FDA 510(k) clearance on 2018-09-05 under approval number K181878. The device is classified under product code OAP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Kiierr 272 Laser, Kiierr 148 Laser?

Kiierr 272 Laser, Kiierr 148 Laser is a medical device that received FDA 510(k) clearance on 2018-09-05. It is manufactured by Kiierr International, LLC. The 510(k) number is K181878.

When was Kiierr 272 Laser, Kiierr 148 Laser approved by the FDA?

Kiierr 272 Laser, Kiierr 148 Laser received FDA 510(k) clearance on 2018-09-05, under approval number K181878.

What company makes Kiierr 272 Laser, Kiierr 148 Laser?

Kiierr 272 Laser, Kiierr 148 Laser is manufactured by Kiierr International, LLC.

What is the FDA product code for Kiierr 272 Laser, Kiierr 148 Laser?

The FDA product code for Kiierr 272 Laser, Kiierr 148 Laser is OAP.

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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.