meddevicedb.com FDA Device Reference

PORTABLE LIMB LOAD MONITOR (BMLLM-100)

K915326 Class I Traditional
Decision Date
1992-10-20
Sponsor / Applicant
Bar Med Pty , Ltd.

Technical Specification

510(k) Submission ID K915326
Product Code IKE
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.1615
Decision Date 1992-10-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PORTABLE LIMB LOAD MONITOR (BMLLM-100) received FDA 510(k) clearance under submission number K915326, sponsored by Bar Med Pty , Ltd.. 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 1992-10-20.

Classification & Regulation

This clearance is catalogued under FDA product code IKE and 21 CFR 890.1615, within the Physical Medicine review panel as a Class I device.