Propper Mfg. Co., Inc. - FDA 510(k) Cleared Devices
Recent clearances: STEAM DOT BLU PROCESS INDICATOR, CLASSIX CHEMICAL STERILIZATION INDICATOR, ONCE-A-DAY VERTOS TEST PACK
25
Total
25
Cleared
0
Denied
FDA 510(k) Regulatory Record - Propper Mfg. Co., Inc. Anesthesiology ✕
1 devices