The following data is part of a premarket notification filed by Ge Healthcare with the FDA for Datex-ohmeda S/5 Cardiac Output Module, E-cop And Accessories.
Device ID | K052976 |
510k Number | K052976 |
Device Name: | DATEX-OHMEDA S/5 CARDIAC OUTPUT MODULE, E-COP AND ACCESSORIES |
Classification | Computer, Diagnostic, Programmable |
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 | DQK |
CFR Regulation Number | 870.1425 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2005-10-24 |
Decision Date | 2006-01-13 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00840682104104 | K052976 | 000 |