INFUSION IV SET
Nov 2001
518d
Nirvi Intl. USA
1
Total
1
Cleared
0
Denied
Nirvi Intl. USA — FDA 510(k) Submissions
Nirvi Intl. USA has submitted 1 FDA 510(k) premarket notifications since 2001, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include I.v. Start Kit . Use the specialty filter in the sidebar to narrow results.
1 devices