Quinton, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PYRAMIS ECG MANAGEMENT SYSTEM MODEL NUMBERS, 92600 AND 92601, QUINTON Q-CATH, MODEL 000460, Q-TEL RMS (REHABILITATION MANAGEMENT SYSTEM), MODEL 000503
164
Total
160
Cleared
0
Denied
FDA 510(k) Regulatory Record - Quinton, Inc. Radiology ✕
3 devices