The following data is part of a premarket notification filed by Body Clock Health Care Ltd with the FDA for Ems 400.
Device ID | K022493 |
510k Number | K022493 |
Device Name: | EMS 400 |
Classification | Stimulator, Muscle, Powered |
Applicant | BODY CLOCK HEALTH CARE LTD 108 GEORGE LANE South Woodford, London, GB E18 1ad |
Contact | Jonathan Bash |
Correspondent | Jonathan Bash BODY CLOCK HEALTH CARE LTD 108 GEORGE LANE South Woodford, London, GB E18 1ad |
Product Code | IPF |
CFR Regulation Number | 890.5850 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2002-07-29 |
Decision Date | 2002-10-11 |
Summary: | summary |