Liofilchem S. R. 1. is one of 126 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
Liofilchem S. R. 1. - FDA 510(k) Cleared Devices
Recent clearances: MTS Lefamulin 0.016- 256 µg/mL
1
Total
1
Cleared
0
Denied
Liofilchem S. R. 1. has 1 FDA 510(k) cleared medical devices. Based in Roseto Degli Abruzzi, IT.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Microbiology.
Browse the FDA 510(k) cleared devices submitted by Liofilchem S. R. 1. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Laboratory Specialists, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Liofilchem S. R. 1.
1 devices