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FDA 510(k)

LineUp

K-Number: K180727 · 2018-05-11

ApplicantCurvebeam, LLC
Decision Date2018-05-11
Product CodeJAK
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LineUp is a medical device manufactured by Curvebeam, LLC. It received FDA 510(k) clearance on 2018-05-11 under approval number K180727. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LineUp?

LineUp is a medical device that received FDA 510(k) clearance on 2018-05-11. It is manufactured by Curvebeam, LLC. The 510(k) number is K180727.

When was LineUp approved by the FDA?

LineUp received FDA 510(k) clearance on 2018-05-11, under approval number K180727.

What company makes LineUp?

LineUp is manufactured by Curvebeam, LLC.

What is the FDA product code for LineUp?

The FDA product code for LineUp is JAK.

Other Devices by Curvebeam, LLC

K170789In Reach K181962CubeVue K203187HiRise K241713HiRise (1040-230)

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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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