The following data is part of a premarket notification filed by Masimo Corporation with the FDA for Lncs Oximetry Sensors.
| Device ID | K083622 |
| 510k Number | K083622 |
| Device Name: | LNCS OXIMETRY SENSORS |
| Classification | Oximeter |
| Applicant | MASIMO CORPORATION 40 PARKER Irvine, CA 92618 |
| Contact | Marguerite Thomlinson |
| Correspondent | Marguerite Thomlinson 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 | 2008-12-08 |
| Decision Date | 2009-04-02 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 10843997002841 | K083622 | 000 |
| 10843997002834 | K083622 | 000 |
| 10843997002827 | K083622 | 000 |
| 10843997002810 | K083622 | 000 |
| 10843997002803 | K083622 | 000 |
| 10843997002797 | K083622 | 000 |