meddevicedb.com FDA Device Reference

MARQUETTE ADULT/NEONATAL WRAP SENSOR

K943817 Class II Traditional
Decision Date
1994-10-18
Sponsor / Applicant
Marquette Electronics, Inc.

Technical Specification

510(k) Submission ID K943817
Product Code DQA
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2700
Decision Date 1994-10-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MARQUETTE ADULT/NEONATAL WRAP SENSOR received FDA 510(k) clearance under submission number K943817, sponsored by Marquette Electronics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1994-10-18.

Classification & Regulation

This clearance is catalogued under FDA product code DQA and 21 CFR 870.2700, within the Cardiovascular review panel as a Class II device.