Seigla Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: LiquID .051 LP Guide Catheter Extension, LiquID 061 Guide Catheter Extension, LiquID 071 Guide Catheter Extension
2
Total
2
Cleared
0
Denied
FDA 510(k) Regulatory Record - Seigla Medical, Inc. Cardiovascular ✕
2 devices