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 |