meddevicedb.com FDA Device Reference

MPS450 MULTIPARAMETER SIMULATOR

K103336 Class II Traditional
Decision Date
2011-04-13
Sponsor / Applicant
Fluke Biomedical

Technical Specification

510(k) Submission ID K103336
Product Code DRT
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2300
Decision Date 2011-04-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MPS450 MULTIPARAMETER SIMULATOR received FDA 510(k) clearance under submission number K103336, sponsored by Fluke Biomedical. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2011-04-13.

Classification & Regulation

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