The following data is part of a premarket notification filed by Shenzhen Jiacom Technology Co., Ltd with the FDA for Wrist Type Automatic Blood Pressure Monitor.
Device ID | K172972 |
510k Number | K172972 |
Device Name: | Wrist Type Automatic Blood Pressure Monitor |
Classification | System, Measurement, Blood-pressure, Non-invasive |
Applicant | Shenzhen Jiacom Technology Co., Ltd No. A6 Building, Silicon Valley Power, Qinghu Park, Longhua Street, Bao'an Dist Shenzhen, CN 518109 |
Contact | Luo Tianfeng |
Correspondent | Diana Hong Mid-Link Consulting Co.,Ltd P.O.Box 120-119 Shanghai, CN 200120 |
Product Code | DXN |
CFR Regulation Number | 870.1130 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-09-26 |
Decision Date | 2018-03-02 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
06953205900771 | K172972 | 000 |
06953205900634 | K172972 | 000 |
06953205900627 | K172972 | 000 |
06953205900610 | K172972 | 000 |
06953205900603 | K172972 | 000 |
06953205900597 | K172972 | 000 |
06953205900580 | K172972 | 000 |
06953205900573 | K172972 | 000 |
06953205900566 | K172972 | 000 |
06953205900559 | K172972 | 000 |
06953205900542 | K172972 | 000 |
06953205900535 | K172972 | 000 |
06953205900641 | K172972 | 000 |
06953205900658 | K172972 | 000 |
06953205900764 | K172972 | 000 |
06953205900757 | K172972 | 000 |
06953205900740 | K172972 | 000 |
06953205900733 | K172972 | 000 |
06953205900726 | K172972 | 000 |
06953205900719 | K172972 | 000 |
06953205900702 | K172972 | 000 |
06953205900696 | K172972 | 000 |
06953205900689 | K172972 | 000 |
06953205900672 | K172972 | 000 |
06953205900665 | K172972 | 000 |
06953205900528 | K172972 | 000 |