Biospace Corporation Limited
FDA 510(k) & PMA Approved Devices — 8 products
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Total Devices8
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K130777 | INBODY | MNW | 2013-11-25 | View |
| 510(k) | K131064 | BIOSPACE | DXN | 2013-09-04 | View |
| 510(k) | K123228 | INBODY 770, INBODY 570, INBODY S10, INBODY H20/INBODY H20(B) | MNW | 2013-03-08 | View |
| 510(k) | K110689 | INBODY | MNW | 2011-08-19 | View |
| 510(k) | K092786 | INBODY, MODELS: 270, R20, R20B | MNW | 2010-03-10 | View |
| 510(k) | K062603 | BIOSPACE BODY COMPOSITION ANALYZERS, MODEL INBODY 230 | MNW | 2007-02-15 | View |
| 510(k) | K052646 | BIOSPACE BODY COMPOSITION ANALYZERS, MODELS INBODY 520, 720 AND S20 | MNW | 2005-12-16 | View |
| 510(k) | K042528 | INBODY, MODEL 3.0 | MNW | 2005-01-11 | View |
No matching devices.
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