Interspec, Inc. - FDA 510(k) Cleared Devices
Recent clearances: INTERSPEC APOGEE RX400 ULTRASOUND IMAGING SYSTEM AND DOPPLER ULTRASOUND FLOWMETER, INTERSPEC APOGEE CLA, INTERSPEC APOGEE ENDO-V PROBE AND NEEDLE GUIDE
17
Total
16
Cleared
0
Denied
FDA 510(k) Regulatory Record - Interspec, Inc. Neurology ✕
2 devices