The following data is part of a premarket notification filed by Bodystat Ltd. with the FDA for Bodystat.
Device ID | K002835 |
510k Number | K002835 |
Device Name: | BODYSTAT |
Classification | Analyzer, Body Composition |
Applicant | BODYSTAT LTD. PO BOX 50 DOUGLAS ISLE OF MAN British Isles, GB Im99 1dq |
Contact | I.j. Meeuwsen |
Correspondent | I.j. Meeuwsen BODYSTAT LTD. PO BOX 50 DOUGLAS ISLE OF MAN British Isles, GB Im99 1dq |
Product Code | MNW |
CFR Regulation Number | 870.2770 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2000-09-12 |
Decision Date | 2001-07-03 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() BODYSTAT 74267832 1817767 Live/Registered |
BODYSTAT LIMITED 1992-04-21 |