Konigsberg Instruments, Inc. - FDA 510(k) Cleared Devices
Recent clearances: MOTILITY PROBE MODEL NUMBERS P31 THRU P38, P40 THRU P43 AND P50
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - Konigsberg Instruments, Inc. Gastroenterology & Urology ✕
2 devices