The following data is part of a premarket notification filed by Spacelabs Healthcare, Inc. with the FDA for Spacelabs Multi-parameter Module.
| Device ID | K103142 |
| 510k Number | K103142 |
| Device Name: | SPACELABS MULTI-PARAMETER MODULE |
| Classification | Detector And Alarm, Arrhythmia |
| Applicant | SPACELABS HEALTHCARE, INC. PO BOX 3018 Nederland, CO 80466 |
| Contact | Thomas Kroenke |
| Correspondent | Thomas Kroenke SPACELABS HEALTHCARE, INC. PO BOX 3018 Nederland, CO 80466 |
| Product Code | DSI |
| Subsequent Product Code | DQA |
| Subsequent Product Code | DSK |
| Subsequent Product Code | DXG |
| Subsequent Product Code | DXN |
| Subsequent Product Code | FLL |
| CFR Regulation Number | 870.1025 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2010-10-25 |
| Decision Date | 2011-03-03 |
| Summary: | summary |