The following data is part of a premarket notification filed by Ge Healthcare with the FDA for Datex-ohmeda S/5 Memory Module, E-mem.
Device ID | K052756 |
510k Number | K052756 |
Device Name: | DATEX-OHMEDA S/5 MEMORY MODULE, E-MEM |
Classification | Monitor, Physiological, Patient(with Arrhythmia Detection Or Alarms) |
Applicant | GE HEALTHCARE 86 PILGRIM ROAD Needham, MA 02492 |
Contact | Joel Kent |
Correspondent | Joel Kent GE HEALTHCARE 86 PILGRIM ROAD Needham, MA 02492 |
Product Code | MHX |
CFR Regulation Number | 870.1025 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2005-09-30 |
Decision Date | 2005-11-01 |
Summary: | summary |