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FDA 510(k), K173214, NES Reprocessed RF Stylet (RFS)
FDA 510(k), K173214, NES Reprocessed RF Stylet (RFS)
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$149.00 USD
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510(K) Number: K173214
Device Name: NES Reprocessed RF Stylet (RFS)
Manufacturer: Northeast Scientific, Inc. (NES)
Device Classification Name: electrosurgical, cutting & coagulation accessories, laparoscopic & endoscopic, reprocessed
Regulation Number: 878.4400
Classification Product Code: NUJ
Date Received: 10/02/2017
Decision Date: 03/27/2018
Regulation Medical Specialty: General & Plastic Surgery
Device Name: NES Reprocessed RF Stylet (RFS)
Manufacturer: Northeast Scientific, Inc. (NES)
Device Classification Name: electrosurgical, cutting & coagulation accessories, laparoscopic & endoscopic, reprocessed
Regulation Number: 878.4400
Classification Product Code: NUJ
Date Received: 10/02/2017
Decision Date: 03/27/2018
Regulation Medical Specialty: General & Plastic Surgery
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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