The following data is part of a premarket notification filed by Dongguan E-test Technology Co., Ltd with the FDA for Automatic Upper Arm Blood Pressure Monitor.
Device ID | K193624 |
510k Number | K193624 |
Device Name: | Automatic Upper Arm Blood Pressure Monitor |
Classification | System, Measurement, Blood-pressure, Non-invasive |
Applicant | Dongguan E-Test Technology Co., Ltd Room 201, 301. Building 1, Changping Section No.1, Dongshen Road Dongguan, CN 523588 |
Contact | Victor Wan |
Correspondent | Cassie Lee DONGGUAN E-TEST TECHNOLOGY CO., LTD Room 201,301. Building 1, Changping Section No. 1 Dongshen Road Dongguan City, CN 523588 |
Product Code | DXN |
CFR Regulation Number | 870.1130 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2019-12-26 |
Decision Date | 2020-07-10 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
06973826010543 | K193624 | 000 |
06973826010536 | K193624 | 000 |