Medtronic Functional Diagnostics A/S - FDA 510(k) Cleared Devices
Recent clearances: NEURO URODYNAMIC SUITE, MODEL 9032E0101, POLYGRAF ID, POLYGRAM '98 ESOPHAGEAL MANOMETRY TESTING APPLICATION, MODELS 9043G0121-9043G0151, 9043S0101, ANORECTAL MANOMETRY SUITE, MODEL 9032S0201
11
Total
11
Cleared
0
Denied
FDA 510(k) Regulatory Record - Medtronic Functional Diagnostics A/S Neurology ✕
2 devices