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NLT — Snare, Flexible, Reprocessed Class II

FDA Device Classification

FDA product code NLT covers "Snare, Flexible, Reprocessed", a Class II medical device regulated under 21 CFR 876.4300. Submissions are reviewed by the Gastroenterology, Urology panel.

Classification Details

Product Code
NLT
Device Class
Class II
Regulation Number
876.4300
Submission Type
Review Panel
GU
Medical Specialty
Gastroenterology, Urology
Implant
No

Definition

Intended to be used endoscopically to snare tissue in preparation for application of electrosurgical current. This device is indicated for reuse/reprocessing. Reprocessing validation data for this device type must be included in a 510(k) submission. (70 FR 56911, available at https://www.govinfo.gov/content/pkg/FR-2005-09-29/pdf/05-19510.pdf).

FDA data resources