The following data is part of a premarket notification filed by Respironics, Inc. with the FDA for Vitalsense Xhr.
| Device ID | K061870 |
| 510k Number | K061870 |
| Device Name: | VITALSENSE XHR |
| Classification | Conditioner, Signal, Physiological |
| Applicant | RESPIRONICS, INC. 1001 MURRY RIDGE LN. Murrysville, PA 15668 |
| Contact | Zita A Yurko |
| Correspondent | Zita A Yurko RESPIRONICS, INC. 1001 MURRY RIDGE LN. Murrysville, PA 15668 |
| Product Code | GWK |
| CFR Regulation Number | 882.1845 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2006-07-03 |
| Decision Date | 2006-08-31 |
| Summary: | summary |