Camntech, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: MOTION WATCH AND PRO-DIARY, ACTIWAVE 1E, ACTIWAVE2E, ACTIWAVE2M, ACTIWAVE4E, ACTIWAVE CARDIO MODEL 08-514, 08-521, 08-536, 08-557, 08-603
2
Total
2
Cleared
0
Denied