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FDA 510(k)

NES Reprocessed RF Stylet (RFS)

K-Number: K173214 · 2018-03-27

Decision Date2018-03-27
Product CodeNUJ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

NES Reprocessed RF Stylet (RFS) is a medical device manufactured by Northeast Scientific, Inc. (Nes). It received FDA 510(k) clearance on 2018-03-27 under approval number K173214. The device is classified under product code NUJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NES Reprocessed RF Stylet (RFS)?

NES Reprocessed RF Stylet (RFS) is a medical device that received FDA 510(k) clearance on 2018-03-27. It is manufactured by Northeast Scientific, Inc. (Nes). The 510(k) number is K173214.

When was NES Reprocessed RF Stylet (RFS) approved by the FDA?

NES Reprocessed RF Stylet (RFS) received FDA 510(k) clearance on 2018-03-27, under approval number K173214.

What company makes NES Reprocessed RF Stylet (RFS)?

NES Reprocessed RF Stylet (RFS) is manufactured by Northeast Scientific, Inc. (Nes).

What is the FDA product code for NES Reprocessed RF Stylet (RFS)?

The FDA product code for NES Reprocessed RF Stylet (RFS) is NUJ.

Related Devices (Code: NUJ)

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.