Millar, Inc. is one of 18443 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Millar, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Mikro-Cath Pressure Catheter
1
Total
1
Cleared
0
Denied
Millar, Inc. has 1 FDA 510(k) cleared medical devices. Based in Houston, US.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Millar, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Acknowledge Regulatory Strategies as regulatory consultant.
FDA 510(k) Regulatory Record - Millar, Inc.
1 devices