eCARTv5 Clinical Deterioration Suite (?eCART?)
Jun 2024
267d
Agilemd, Inc.
1
Total
1
Cleared
0
Denied
Agilemd, Inc. — FDA 510(k) Submissions
Agilemd, Inc. has submitted 1 FDA 510(k) premarket notifications since 2024, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Medium-term Adjunctive Predictive Cardiovascular Indicator . Use the specialty filter in the sidebar to narrow results.
1 devices