meddevicedb.com FDA Device Reference

Permanent Sled Bag

K152403 Class II Special
Decision Date
2015-09-22
Sponsor / Applicant
Boston Scientific

Technical Specification

510(k) Submission ID K152403
Product Code ITX
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1570
Decision Date 2015-09-22
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Permanent Sled Bag received FDA 510(k) clearance under submission number K152403, sponsored by Boston Scientific. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2015-09-22.

Classification & Regulation

This clearance is catalogued under FDA product code ITX and 21 CFR 892.1570, within the Radiology review panel as a Class II device.