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PLANET MONITORING SYSTEM

K032871 Class II Traditional
Decision Date
2003-11-10
Sponsor / Applicant
Larsen & Toubro Limited

Technical Specification

510(k) Submission ID K032871
Product Code MWI
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2300
Decision Date 2003-11-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PLANET MONITORING SYSTEM received FDA 510(k) clearance under submission number K032871, sponsored by Larsen & Toubro Limited. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2003-11-10.

Classification & Regulation

This clearance is catalogued under FDA product code MWI and 21 CFR 870.2300, within the Cardiovascular review panel as a Class II device.