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PHYSICAL MONITORING REGISTRATION UNIT-S (PMRU-S)

K123902 Class II Traditional
Decision Date
2013-09-13
Sponsor / Applicant
Oktx, LLC

Technical Specification

510(k) Submission ID K123902
Product Code IKN
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.1375
Decision Date 2013-09-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PHYSICAL MONITORING REGISTRATION UNIT-S (PMRU-S) received FDA 510(k) clearance under submission number K123902, sponsored by Oktx, 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 2013-09-13.

Classification & Regulation

This clearance is catalogued under FDA product code IKN and 21 CFR 890.1375, within the Physical Medicine review panel as a Class II device.