The following data is part of a premarket notification filed by Masimo Corporation with the FDA for Masimo Set And Masimo Rainbow Set Pulse Oximeters And Sensors.
| Device ID | K120657 |
| 510k Number | K120657 |
| Device Name: | MASIMO SET AND MASIMO RAINBOW SET PULSE OXIMETERS AND SENSORS |
| Classification | Oximeter |
| Applicant | MASIMO CORPORATION 40 PARKER Irvine, CA 92618 |
| Contact | Patricia Milbank |
| Correspondent | Patricia Milbank MASIMO CORPORATION 40 PARKER Irvine, CA 92618 |
| Product Code | DQA |
| CFR Regulation Number | 870.2700 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-03-05 |
| Decision Date | 2012-09-19 |
| Summary: | summary |