meddevicedb.com FDA Device Reference

SD-700 BLOOD PRESSURE MONITOR

K802201 Class II Traditional
Decision Date
1980-10-23
Sponsor / Applicant
Industrial & Biomedical Sensors Corp.

Technical Specification

510(k) Submission ID K802201
Product Code DXN
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1130
Decision Date 1980-10-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SD-700 BLOOD PRESSURE MONITOR received FDA 510(k) clearance under submission number K802201, sponsored by Industrial & Biomedical Sensors Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1980-10-23.

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.