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PYTHON AMBULATORY BLOOD PRESSURE MONITORING SYSTEM

K874917 Class II Traditional
Decision Date
1988-05-10
Sponsor / Applicant
Oxford Medilog, Inc.

Technical Specification

510(k) Submission ID K874917
Product Code DXN
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1130
Decision Date 1988-05-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PYTHON AMBULATORY BLOOD PRESSURE MONITORING SYSTEM received FDA 510(k) clearance under submission number K874917, sponsored by Oxford Medilog, 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 1988-05-10.

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.