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OSCILLOMATE NON-INVASIVE BLOOD PRESSURE MONITOR

K972020 Class II Traditional
Decision Date
1998-05-05
Sponsor / Applicant
Cas Medical Systems, Inc.

Technical Specification

510(k) Submission ID K972020
Product Code DXW
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1270
Decision Date 1998-05-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OSCILLOMATE NON-INVASIVE BLOOD PRESSURE MONITOR received FDA 510(k) clearance under submission number K972020, sponsored by Cas Medical Systems, 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 1998-05-05.

Classification & Regulation

This clearance is catalogued under FDA product code DXW and 21 CFR 870.1270, within the Cardiovascular review panel as a Class II device.