meddevicedb.com FDA Device Reference

RAPID STRAND RX

K122764 Class II Traditional
Decision Date
2012-12-28
Sponsor / Applicant
Medi-Physics, Inc.

Technical Specification

510(k) Submission ID K122764
Product Code KXK
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.5730
Decision Date 2012-12-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RAPID STRAND RX received FDA 510(k) clearance under submission number K122764, sponsored by Medi-Physics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2012-12-28.

Classification & Regulation

This clearance is catalogued under FDA product code KXK and 21 CFR 892.5730, within the Radiology review panel as a Class II device.