The following data is part of a premarket notification filed by Hewlett-packard Gmbh with the FDA for Hp Viridia Cms Patient Monitor With Eeg Parameter, Model M1027a.
Device ID | K992674 |
510k Number | K992674 |
Device Name: | HP VIRIDIA CMS PATIENT MONITOR WITH EEG PARAMETER, MODEL M1027A |
Classification | Monitor, Physiological, Patient(with Arrhythmia Detection Or Alarms) |
Applicant | HEWLETT-PACKARD GMBH HERRENBERGER STR. 110-140 Boeblingen, DE 71034 |
Contact | Egon Pfeil |
Correspondent | Egon Pfeil HEWLETT-PACKARD GMBH HERRENBERGER STR. 110-140 Boeblingen, DE 71034 |
Product Code | MHX |
CFR Regulation Number | 870.1025 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Abbreviated |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1999-08-10 |
Decision Date | 1999-11-08 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00884838021075 | K992674 | 000 |
00884838011908 | K992674 | 000 |
00884838011878 | K992674 | 000 |
00884838011861 | K992674 | 000 |
20884838011896 | K992674 | 000 |