The following data is part of a premarket notification filed by Nonin Medical, Inc. with the FDA for 4100 Patient Oximeter Module.
| Device ID | K043359 |
| 510k Number | K043359 |
| Device Name: | 4100 PATIENT OXIMETER MODULE |
| Classification | Oximeter |
| Applicant | NONIN MEDICAL, INC. 2605 FERNBROOK LANE, NORTH Minneapolis, MN 55447 -4755 |
| Contact | John R Dalpee |
| Correspondent | John R Dalpee NONIN MEDICAL, INC. 2605 FERNBROOK LANE, NORTH Minneapolis, MN 55447 -4755 |
| Product Code | DQA |
| CFR Regulation Number | 870.2700 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2004-12-06 |
| Decision Date | 2005-01-07 |
| Summary: | summary |