meddevicedb.com FDA Device Reference

SPHYGMOCOR MX MODEL SCOR-MX

K002742 Class II Traditional
Decision Date
2001-05-01
Sponsor / Applicant
Pwv Medical Pty, Lt.

Technical Specification

510(k) Submission ID K002742
Product Code DSK
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1110
Decision Date 2001-05-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SPHYGMOCOR MX MODEL SCOR-MX received FDA 510(k) clearance under submission number K002742, sponsored by Pwv Medical Pty, Lt.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2001-05-01.

Classification & Regulation

This clearance is catalogued under FDA product code DSK and 21 CFR 870.1110, within the Cardiovascular review panel as a Class II device.