Hewlett-Packard Co. - FDA 510(k) Cleared Devices
Recent clearances: HEARTSTREAM XLT DEFIBRILLATOR/MONITOR, AC CHARGER, DC CHARGER, DATA CARD, SINGLE BAY ADAPTER, DEFIBRILLATOR PADS CABLE, HP M2376A DEVICE LINK SYSTEM, MODIFICATION OF: PHYSIOLOGICAL SIGNAL TRANSMITTER AND RECEIVER, MODEL 3810A
230
Total
229
Cleared
0
Denied
FDA 510(k) Regulatory Record - Hewlett-Packard Co. General & Plastic Surgery ✕
1 devices