meddevicedb.com FDA Device Reference

EZ-ASSIST-FILL

K121661 Class I Traditional
Decision Date
2012-12-27
Sponsor / Applicant
Assist Fill, LLC

Technical Specification

510(k) Submission ID K121661
Product Code PCM
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5050
Decision Date 2012-12-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EZ-ASSIST-FILL received FDA 510(k) clearance under submission number K121661, sponsored by Assist Fill, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 2012-12-27.

Classification & Regulation

This clearance is catalogued under FDA product code PCM and 21 CFR 890.5050, within the Physical Medicine review panel as a Class I device.