OSPREY MEDICAL, INC
FDA Registration(s)#
| Registration | FEI | Name | Status | Initial importer | Expiration year | Address |
|---|---|---|---|---|---|---|
| 3010368762 | 3010368762 | OSPREY MEDICAL, INC | 1 | N | 2020-04-25 | 5600 Rowland Rd Suite 250 Minnetonka MN US 55343 |
Registered Device Listings#
| Registration key | Listing key | Premarket submission | Device | Product code | Decision date |
|---|---|---|---|---|---|
| 162113 | 2061851978 | K190102 | DyeVert™ Plus Contrast Reduction System, DyeTect™ Contrast Monitoring System, DyeVert™ Plus EZ Contrast Reduction System | DXT | 2019-10-17 |
| 162113 | 1385514190 | K181936 | DyeVert PLUS EZ Contrast Reduction System | DXT | 2018-10-25 |
| 162113 | 1330152549 | K171698 | Smart Syringe | DXT | 2017-07-07 |
| 162113 | 1456339945 | K163054 | DyeVert Plus Contrast Modulation/Monitoring System, Contrast Monitoring System | DXT | 2017-03-08 |
Product Codes Associated With Registrations#
| Product code | Registration listing records | Latest decision |
|---|---|---|
| DXT | 4 | 2019-10-17 |