The following data is part of a premarket notification filed by Shenzhen Healthcare Electronic Technology Co. Ltd with the FDA for Body Analysis Scale.
Device ID | K112951 |
510k Number | K112951 |
Device Name: | BODY ANALYSIS SCALE |
Classification | Analyzer, Body Composition |
Applicant | SHENZHEN HEALTHCARE ELECTRONIC TECHNOLOGY CO. LTD 77325 JOYCE WAY Echo, OR 97826 |
Contact | Charlie Mack |
Correspondent | Charlie Mack SHENZHEN HEALTHCARE ELECTRONIC TECHNOLOGY CO. LTD 77325 JOYCE WAY Echo, OR 97826 |
Product Code | MNW |
CFR Regulation Number | 870.2770 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2011-10-04 |
Decision Date | 2011-11-01 |