FDA 510(k), K090661, NES REPROCESSED VARICOSE VEIN RF CATHETER

FDA 510(k), K090661, NES REPROCESSED VARICOSE VEIN RF CATHETER

Regular price $49.00 USD
Regular price Sale price $49.00 USD
Sale Sold out
510(K) Number: K090661
Device Name: NES REPROCESSED VARICOSE VEIN RF CATHETER
Manufacturer: CRAIG ALLMENDINGER
Device Classification Name: Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
Regulation Number: NUJ
Classification Product Code: KXA
Date Received: 03/12/2009
Decision Date: 07/21/2010
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery
  • Status: Pending Fast-Track Request
  • Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity

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.

View full details