TransFix/EDTA Vacuum Blood Collection Tubes
Jun 2017
266d
Caltag Medsystems, Ltd.
1
Total
1
Cleared
0
Denied
Caltag Medsystems, Ltd. — FDA 510(k) Submissions
Caltag Medsystems, Ltd. has submitted 1 FDA 510(k) premarket notifications since 2017, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Tubes, Vacuum Sample, With Anticoagulant . Use the specialty filter in the sidebar to narrow results.
1 devices