FDA 510(k) Applications Submitted by BIOSPACE CORPORATION LIMITED
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K110689 |
03/15/2011 |
INBODY |
BIOSPACE CORPORATION LIMITED |
| K131064 |
04/16/2013 |
BIOSPACE |
BIOSPACE CORPORATION LIMITED |
| K141483 |
06/05/2014 |
BIOSPACE BODY COMPOSITION ANALYZER |
BIOSPACE CORPORATION LIMITED |
| K062603 |
09/01/2006 |
BIOSPACE BODY COMPOSITION ANALYZERS, MODEL INBODY 230 |
BIOSPACE CORPORATION LIMITED |
| K092786 |
09/10/2009 |
INBODY, MODELS: 270, R20, R20B |
BIOSPACE CORPORATION LIMITED |
| K042528 |
09/17/2004 |
INBODY, MODEL 3.0 |
BIOSPACE CORPORATION LIMITED |
| K052646 |
09/26/2005 |
BIOSPACE BODY COMPOSITION ANALYZERS, MODELS INBODY 520, 720 AND S20 |
BIOSPACE CORPORATION LIMITED |
| K123228 |
10/15/2012 |
INBODY 770, INBODY 570, INBODY S10, INBODY H20/INBODY H20(B) |
BIOSPACE CORPORATION LIMITED |
| K130777 |
03/21/2013 |
INBODY |
BIOSPACE CORPORATION LIMITED |
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