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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 the device name listed in this FDA 510(k) record. The listed applicant is Northeast Scientific, Inc. (Nes). It received FDA 510(k) clearance on 2018-03-27 under 510(k) 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. The listed applicant is Northeast Scientific, Inc. (Nes). The 510(k) number is K173214.

When did NES Reprocessed RF Stylet (RFS) receive FDA 510(k) clearance?

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

Who is the listed applicant for NES Reprocessed RF Stylet (RFS)?

The FDA 510(k) record lists Northeast Scientific, Inc. (Nes) as the applicant. This does not by itself establish the device manufacturer.

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)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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