meddevicedb.com FDA Device Reference

SHIELD DISPOSABLE BLOOD PRESSURE CUFF

K801568 Class II Traditional
Decision Date
1980-07-28
Sponsor / Applicant
American Convertors Div., American Pharmaseal

Technical Specification

510(k) Submission ID K801568
Product Code DXQ
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1120
Decision Date 1980-07-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SHIELD DISPOSABLE BLOOD PRESSURE CUFF received FDA 510(k) clearance under submission number K801568, sponsored by American Convertors Div., American Pharmaseal. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1980-07-28.

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.