The following data is part of a premarket notification filed by Suntech Medical, Inc. with the FDA for Oscar 2.
| Device ID | K151520 |
| 510k Number | K151520 |
| Device Name: | Oscar 2 |
| Classification | System, Measurement, Blood-pressure, Non-invasive |
| Applicant | SunTech Medical, Inc. 507 Airport Blvd, Suite 117 Morrisville, NC 27560 |
| Contact | Charles Setzer |
| Correspondent | Charles Setzer SunTech Medical, Inc. 507 Airport Blvd, Suite 117 Morrisville, NC 27560 |
| Product Code | DXN |
| CFR Regulation Number | 870.1130 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Abbreviated |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2015-06-05 |
| Decision Date | 2016-02-19 |
| Summary: | summary |