meddevicedb.com FDA Device Reference

sam X1 Long Duration Ultrasound Device

K211513 Class II Special
Decision Date
2021-08-18
Sponsor / Applicant
ZetrOZ Systems, LLC

Technical Specification

510(k) Submission ID K211513
Product Code PFW
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5300
Decision Date 2021-08-18
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

sam X1 Long Duration Ultrasound Device received FDA 510(k) clearance under submission number K211513, sponsored by ZetrOZ Systems, LLC. The device was reviewed via the Special premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 2021-08-18.

Classification & Regulation

This clearance is catalogued under FDA product code PFW and 21 CFR 890.5300, within the Physical Medicine review panel as a Class II device.