The following data is part of a premarket notification filed by Finapres Medical Systems Bv with the FDA for Finapres Nova Noninvasive Hemodynamic Monitor.
Device ID | K141460 |
510k Number | K141460 |
Device Name: | FINAPRES NOVA NONINVASIVE HEMODYNAMIC MONITOR |
Classification | System, Measurement, Blood-pressure, Non-invasive |
Applicant | FINAPRES MEDICAL SYSTEMS BV HOGEHILWEG 8 Amsterdam, NL 1101 Cc |
Contact | Ir. Paul Kosters |
Correspondent | Ir. Paul Kosters FINAPRES MEDICAL SYSTEMS BV HOGEHILWEG 8 Amsterdam, NL 1101 Cc |
Product Code | DXN |
CFR Regulation Number | 870.1130 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2014-06-02 |
Decision Date | 2015-03-20 |
Summary: | summary |