meddevicedb.com FDA Device Reference

Resolution Clip

K151802 Class II Traditional
Decision Date
2015-08-06
Sponsor / Applicant
Boston Scientific Corporation

Technical Specification

510(k) Submission ID K151802
Product Code PKL
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.4400
Decision Date 2015-08-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Resolution Clip received FDA 510(k) clearance under submission number K151802, sponsored by Boston Scientific Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2015-08-06.

Classification & Regulation

This clearance is catalogued under FDA product code PKL and 21 CFR 876.4400, within the Gastroenterology, Urology review panel as a Class II device.