KAEN YIH UMBILICAL CORD CLAMP
Mar 2004
91d
Kaen Yih Enterprise Co., Ltd.
1
Total
1
Cleared
0
Denied
Kaen Yih Enterprise Co., Ltd. — FDA 510(k) Submissions
Kaen Yih Enterprise Co., Ltd. has submitted 1 FDA 510(k) premarket notifications since 2004, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Clamp, Umbilical . Use the specialty filter in the sidebar to narrow results.
1 devices