Hewlett-Packard Co.
Hewlett-Packard Co. — FDA 510(k) Submissions
Hewlett-Packard Co. has submitted 230 FDA 510(k) premarket notifications since 1976, of which 229 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Monitor, Cardiac (incl. Cardiotachometer & Rate Alarm), Detector And Alarm, Arrhythmia, System, Imaging, Pulsed Echo, Ultrasonic, Electrocardiograph, System, Monitoring, Perinatal . Use the specialty filter in the sidebar to narrow results.
Looking for a specific device from Hewlett-Packard Co.? Search by device name or K-number.
Search all Hewlett-Packard Co. devices