The following data is part of a premarket notification filed by Nihon Kohden America, Inc. with the FDA for Nihon Kohden Bedside Monitor, Model Bsm-6000s Series.
Device ID | K080342 |
510k Number | K080342 |
Device Name: | NIHON KOHDEN BEDSIDE MONITOR, MODEL BSM-6000S SERIES |
Classification | Monitor, Physiological, Patient(with Arrhythmia Detection Or Alarms) |
Applicant | NIHON KOHDEN AMERICA, INC. 90 ICON ST. Foothill Ranch, CA 92610 -1601 |
Contact | Jack Coggan |
Correspondent | Jack Coggan NIHON KOHDEN AMERICA, INC. 90 ICON ST. Foothill Ranch, CA 92610 -1601 |
Product Code | MHX |
CFR Regulation Number | 870.1025 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2008-02-08 |
Decision Date | 2008-02-26 |
Summary: | summary |