The following data is part of a premarket notification filed by Shenzhen Mindray Bio-meidcal Electronics Co., Ltd with the FDA for Passport Series Patient Monitors (including Passport 17m, Passport 12m And T1).
Device ID | K143195 |
510k Number | K143195 |
Device Name: | Passport Series Patient Monitors (including Passport 17M, Passport 12M And T1) |
Classification | Monitor, Physiological, Patient(with Arrhythmia Detection Or Alarms) |
Applicant | Shenzhen Mindray Bio-Meidcal Electronics Co., Ltd Mindray Building, Keji 12th Road South Hi-tech Industrial Park Shenzhen, TW 518057 |
Contact | Yanhong Bai |
Correspondent | Yanhong Bai Shenzhen Mindray Bio-Meidcal Electronics Co., Ltd Mindray Building, Keji 12th Road South Hi-tech Industrial Park Shenzhen, TW 518057 |
Product Code | MHX |
CFR Regulation Number | 870.1025 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2014-11-06 |
Decision Date | 2014-12-22 |
Summary: | summary |