Pacesetter, Inc. - FDA 510(k) Cleared Devices
Recent clearances: LOCATOR MODEL 4036, SIEMENS SERVO ULTRA NEBULIZER 345, AFP CARDIAC PACING SYSTEM MODEL 283 (MODIFICATION)
8
Total
2
Cleared
0
Denied
FDA 510(k) Regulatory Record - Pacesetter, Inc. Anesthesiology ✕
1 devices