The following data is part of a premarket notification filed by Nellcor Puritan Bennett, Inc. with the FDA for Oximax N-550 Pulse Oximeter,model N-550 Pulse Oximeter.
| Device ID | K021090 |
| 510k Number | K021090 |
| Device Name: | OXIMAX N-550 PULSE OXIMETER,MODEL N-550 PULSE OXIMETER |
| Classification | Oximeter |
| Applicant | NELLCOR PURITAN BENNETT, INC. 4280 HACIENDA DR. Pleasanton, CA 94588 -2719 |
| Contact | Gina To |
| Correspondent | Gina To NELLCOR PURITAN BENNETT, INC. 4280 HACIENDA DR. Pleasanton, CA 94588 -2719 |
| Product Code | DQA |
| CFR Regulation Number | 870.2700 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2002-04-04 |
| Decision Date | 2002-05-08 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 10884521582538 | K021090 | 000 |
| 10884521582484 | K021090 | 000 |