The following data is part of a premarket notification filed by Health & Life Co., Ltd. with the FDA for Full Automatic (nibp) Blood Pressure Monitor.
Device ID | K160336 |
510k Number | K160336 |
Device Name: | Full Automatic (NIBP) Blood Pressure Monitor |
Classification | System, Measurement, Blood-pressure, Non-invasive |
Applicant | Health & Life Co., Ltd. 9F, No. 186, Jian Yi Road Zhonghe District, New Taipei City, CN 23553 |
Contact | Sarah Su |
Correspondent | Sarah Su Health & Life Co., Ltd. 9F, No. 186, Jian Yi Road Zhonghe District, New Taipei City, CN 23553 |
Product Code | DXN |
CFR Regulation Number | 870.1130 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-02-08 |
Decision Date | 2016-03-29 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
10311917194643 | K160336 | 000 |
10311917183364 | K160336 | 000 |
04719872480198 | K160336 | 000 |
14719872480027 | K160336 | 000 |
14719872480010 | K160336 | 000 |