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CLEARMEDICAL/CRITIKON BLOOD PRESSURE CUFF; CLEARMEDICAL/WELCH ALLYN BLOOD PRESSURE CUFF

K031416 Class II Traditional
Decision Date
2003-07-15
Sponsor / Applicant
Clearmedical, Inc.

Technical Specification

510(k) Submission ID K031416
Product Code DXQ
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1120
Decision Date 2003-07-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CLEARMEDICAL/CRITIKON BLOOD PRESSURE CUFF; CLEARMEDICAL/WELCH ALLYN BLOOD PRESSURE CUFF received FDA 510(k) clearance under submission number K031416, sponsored by Clearmedical, 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 2003-07-15.

Classification & Regulation

This clearance is catalogued under FDA product code DXQ and 21 CFR 870.1120, within the Cardiovascular review panel as a Class II device.