PAIN VISION, MODEL PS-2100
Jan 2009
457d
Osachi Co., Ltd.
1
Total
1
Cleared
0
Denied
Osachi Co., Ltd. — FDA 510(k) Submissions
Osachi Co., Ltd. has submitted 1 FDA 510(k) premarket notifications since 2009, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Device, Vibration Threshold Measurement . Use the specialty filter in the sidebar to narrow results.
1 devices