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NELLCOR SYMPHONY N-3100 BLOOD PRESSURE MONITOR

K953472 Class II Traditional
Decision Date
1995-10-20
Sponsor / Applicant
Nellcor, Inc.

Technical Specification

510(k) Submission ID K953472
Product Code DXN
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1130
Decision Date 1995-10-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NELLCOR SYMPHONY N-3100 BLOOD PRESSURE MONITOR received FDA 510(k) clearance under submission number K953472, sponsored by Nellcor, 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 1995-10-20.

Classification & Regulation

This clearance is catalogued under FDA product code DXN and 21 CFR 870.1130, within the Cardiovascular review panel as a Class II device.