The following data is part of a premarket notification filed by Osprey Medical, Inc. with the FDA for Contrast Monitoring System Display, Contrast Monitoring System Syringes.
| Device ID | K142081 |
| 510k Number | K142081 |
| Device Name: | CONTRAST MONITORING SYSTEM DISPLAY, CONTRAST MONITORING SYSTEM SYRINGES |
| Classification | Injector And Syringe, Angiographic |
| Applicant | OSPREY MEDICAL, INC. 5600 ROWLAND ROAD SUITE 250 Minnetonka, MN 55343 |
| Contact | Melanie Hess |
| Correspondent | Melanie Hess OSPREY MEDICAL, INC. 5600 ROWLAND ROAD SUITE 250 Minnetonka, MN 55343 |
| Product Code | DXT |
| CFR Regulation Number | 870.1650 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2014-07-31 |
| Decision Date | 2014-12-12 |
| Summary: | summary |