Monitor, Patient (Model 78331A)

by Hewlett-Packard Co. 510(k)

Active United States

510(k) K760150

Regulatory status

as of 28 Oct 2026

Region	Authorization	Number	Date	Status
United States	FDA 510(k)SESE Substantially Equivalent · Traditional	NumberK760150	Date19 Jul 1976Cleared	StatusActive

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not known
Not covered

United States — FDA 510(k) Active

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

510(k)

510(k) Number: K760150
FDA Product Code: DPS

Device Class: Class II
Regulation: 21 CFR Part 870.2340
Advisory Committee: Cardiovascular
FDA Decision: SESE Substantially Equivalent

Other devices from Hewlett-Packard Co.

Luer Lock Skirt

Class II
Hp Sonos 100 Cf Ultrasound Imaging System

Class II
Medical Diag. Ultrasound Instr. 77065

Class II
Model M1403A Telemetry Monitoring Systems (TMS)

Class II
Differential Refractive Index Detector

Class I
Model 80100A, Patient Data Memory

Class II

See all devices from Hewlett-Packard Co. →