Medrad, Inc. - FDA 510(k) Cleared Devices
Recent clearances: JETSTREAM XC 2.4/3.4, ANGIOJET ULTRA POWER PULSE KIT, JETSTREAM XC 2.4/3.4 SYSTEM
105
Total
105
Cleared
0
Denied
FDA 510(k) Regulatory Record - Medrad, Inc. Toxicology ✕
2 devices