Cbc Corp. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - Cbc Corp. Neurology ✕
5 devices
Cleared
Aug 31, 1983
AUTO-TENS MODEL V
Neurology
44d
Cleared
Mar 07, 1983
AUTO-TENS MODEL III DUAL CHANNEL REPLACE
Neurology
108d
Cleared
Feb 07, 1983
AUTO-TENS MODEL I DISPOS. SINGLE CHAN
Neurology
80d
Cleared
Feb 02, 1983
AUTO-TENS MODEL IV -DUAL CHANNEL FULL
Neurology
75d
Cleared
Feb 02, 1983
AUTO-TENS MODEL II SINGLE CHANNEL
Neurology
75d