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Cbc Corp.

FDA 510(k) & PMA Approved Devices — 5 products

Total Devices5

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K832337	AUTO-TENS MODEL V	GZJ	1983-08-31	View
510(k)	K823466	AUTO-TENS MODEL III DUAL CHANNEL REPLACE	GZJ	1983-03-07	View
510(k)	K823467	AUTO-TENS MODEL I DISPOS. SINGLE CHAN	GZJ	1983-02-07	View
510(k)	K823465	AUTO-TENS MODEL II SINGLE CHANNEL	GZJ	1983-02-02	View
510(k)	K823464	AUTO-TENS MODEL IV -DUAL CHANNEL FULL	GZJ	1983-02-02	View

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