The following data is part of a premarket notification filed by Edan Instruments, Inc. with the FDA for Electrocardiograph.
Device ID | K170995 |
510k Number | K170995 |
Device Name: | Electrocardiograph |
Classification | Electrocardiograph |
Applicant | Edan Instruments, Inc. #15 Jinhui Road, Jinsha Community, Kengzi Sub-District Shenzhen, CN 518122 |
Contact | Alice Yang |
Correspondent | Doug Worth Edan Medical 1200 Crossman Ave, Suite 200 Sunnyvale, CA 94086 |
Product Code | DPS |
CFR Regulation Number | 870.2340 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-04-03 |
Decision Date | 2017-06-02 |
Summary: | summary |