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FDA 510(k)

Advantage Plus Pass-Thru

K-Number: K172677 · 2017-12-19

Decision Date2017-12-19
Product CodeFEB
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Advantage Plus Pass-Thru is a medical device manufactured by Medivators, Inc.. It received FDA 510(k) clearance on 2017-12-19 under approval number K172677. The device is classified under product code FEB. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Advantage Plus Pass-Thru?

Advantage Plus Pass-Thru is a medical device that received FDA 510(k) clearance on 2017-12-19. It is manufactured by Medivators, Inc.. The 510(k) number is K172677.

When was Advantage Plus Pass-Thru approved by the FDA?

Advantage Plus Pass-Thru received FDA 510(k) clearance on 2017-12-19, under approval number K172677.

What company makes Advantage Plus Pass-Thru?

Advantage Plus Pass-Thru is manufactured by Medivators, Inc..

What is the FDA product code for Advantage Plus Pass-Thru?

The FDA product code for Advantage Plus Pass-Thru is FEB.

Other Devices by Medivators, Inc.

Related Devices (Code: FEB)

Official Source

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