Lkb Instruments, Inc. - FDA 510(k) Cleared Devices
Recent clearances: 1205 BETAPLATE LIQUID SCINTILLATION COUNTER, DELFIA(TM) FERRITIN KIT, DELFIA(TM) THYROXINE (T4) KIT
52
Total
52
Cleared
0
Denied
FDA 510(k) Regulatory Record - Lkb Instruments, Inc. Hematology ✕
4 devices