The following data is part of a premarket notification filed by Nellcor Puritan Bennett, Inc. with the FDA for Duramax Reusable Oximetry Sensor.
| Device ID | K070408 |
| 510k Number | K070408 |
| Device Name: | DURAMAX REUSABLE OXIMETRY SENSOR |
| Classification | Oximeter |
| Applicant | NELLCOR PURITAN BENNETT, INC. 4280 HACIENDA DR. Pleasanton, CA 94588 -2719 |
| Contact | James Bonds |
| Correspondent | James Bonds NELLCOR PURITAN BENNETT, INC. 4280 HACIENDA DR. Pleasanton, CA 94588 -2719 |
| Product Code | DQA |
| CFR Regulation Number | 870.2700 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Abbreviated |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2007-02-12 |
| Decision Date | 2007-05-25 |
| Summary: | summary |