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FDA 510(k)

NemoScan

K-Number: K192571 · 2019-12-11

ApplicantSoftware Nemotec S.L.
Decision Date2019-12-11
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

NemoScan is a medical device manufactured by Software Nemotec S.L.. It received FDA 510(k) clearance on 2019-12-11 under approval number K192571. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NemoScan?

NemoScan is a medical device that received FDA 510(k) clearance on 2019-12-11. It is manufactured by Software Nemotec S.L.. The 510(k) number is K192571.

When was NemoScan approved by the FDA?

NemoScan received FDA 510(k) clearance on 2019-12-11, under approval number K192571.

What company makes NemoScan?

NemoScan is manufactured by Software Nemotec S.L..

What is the FDA product code for NemoScan?

The FDA product code for NemoScan is LLZ.

Other Devices by Software Nemotec S.L.

K193003NemoCast K192475NemoFAB K232549NemoCast K232698NemoScan

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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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