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FDA 510(k)

nextaro® v, 20/20

K-Number: K240748 · 2024-04-16

ApplicantSfm Medical Devices GmbH
Decision Date2024-04-16
Product CodeLHI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

nextaro® v, 20/20 is a medical device manufactured by Sfm Medical Devices GmbH. It received FDA 510(k) clearance on 2024-04-16 under approval number K240748. The device is classified under product code LHI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the nextaro® v, 20/20?

nextaro® v, 20/20 is a medical device that received FDA 510(k) clearance on 2024-04-16. It is manufactured by Sfm Medical Devices GmbH. The 510(k) number is K240748.

When was nextaro® v, 20/20 approved by the FDA?

nextaro® v, 20/20 received FDA 510(k) clearance on 2024-04-16, under approval number K240748.

What company makes nextaro® v, 20/20?

nextaro® v, 20/20 is manufactured by Sfm Medical Devices GmbH.

What is the FDA product code for nextaro® v, 20/20?

The FDA product code for nextaro® v, 20/20 is LHI.

Other Devices by Sfm Medical Devices GmbH

K183187nextaro Transfer System, nextaro va K241976nextaro® va, 15mm, 5µm

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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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