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MODELS M1175A & M1176A COMPONENT MONITORING SYSTEM

K882609 Class II Traditional
Decision Date
1989-01-19
Sponsor / Applicant
Waltham Div. Hewlett Packard

Technical Specification

510(k) Submission ID K882609
Product Code DRT
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2300
Decision Date 1989-01-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODELS M1175A & M1176A COMPONENT MONITORING SYSTEM received FDA 510(k) clearance under submission number K882609, sponsored by Waltham Div. Hewlett Packard. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1989-01-19.

Classification & Regulation

This clearance is catalogued under FDA product code DRT and 21 CFR 870.2300, within the Cardiovascular review panel as a Class II device.