The following data is part of a premarket notification filed by Truly Instrument Limited with the FDA for Automatic Arm Bluetooth Blood Pressure Monitor.
Device ID | K161846 |
510k Number | K161846 |
Device Name: | Automatic Arm Bluetooth Blood Pressure Monitor |
Classification | System, Measurement, Blood-pressure, Non-invasive |
Applicant | TRULY INSTRUMENT LIMITED SITE 2, TRULY INDUSTRY AREA Shanwei, CN 516600 |
Contact | Yang Jian-ho |
Correspondent | Max Wong TRULY (U.S.A) INC 2620 CONCORD AVENUE, SUITE 106 Alhambra, CA 91803 |
Product Code | DXN |
CFR Regulation Number | 870.1130 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Abbreviated |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-07-05 |
Decision Date | 2016-10-24 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
34719878120037 | K161846 | 000 |