This page includes the latest FDA filings for Seastar Medical Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 3015045325 |
| FEI Number | 3015045325 |
| Name | SEASTAR MEDICAL, INC. |
| Owner & Operator | SeaStar Medical, Inc. |
| Contact Address | 3513 Brighton Blvd Suite 410 Denver CO 80216 US |
| Official Correspondent |
|
| Registration Status | 1 |
| Initial Importer | N |
| Registration Expiration | 2020-04-25 |
| Registration Address | 2187 Newcastle Ave. Suite 200 Cardiff by the Sea, CA 92007 US |
| Establishment Type | Repack or Relabel Medical Device |
Device Company | Device | Date |
|---|---|---|
| SEASTAR MEDICAL INCORPORATED | Quelimmune 02-1006-01 | 2024-05-29 |
| SEASTAR MEDICAL, INC. | CLR CLR 2.0 | 2019-06-19 |
SEASTAR MEDICAL, INC. | CLR 2.0 Hemofilter | 2018-11-08 |
| NCAGE Code | 5JV11 | SEASTAR MEDICAL, INC. |
| CAGE Code | 5JV11 | SEASTAR MEDICAL, INC. |
| S.A.M. Registration | 5JV11 [21721920] | SEASTAR MEDICAL, INC. |