Barosense, Inc.
FDA 510(k) & PMA Approved Devices — 5 products
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Total Devices5
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K120126 | BAROSENSE ENDOGASTRIC TUBE AND INTRODUCER BOUGIE | FED | 2012-09-10 | View |
| 510(k) | K120147 | ACE STAPLER AND CARTRIDGE | OCW | 2012-02-17 | View |
| 510(k) | K110829 | ACE STAPLER AND CARTRIDGE | OCW | 2011-06-03 | View |
| 510(k) | K082044 | ACE STAPLER, MODEL F0031 | OCW | 2010-05-11 | View |
| 510(k) | K082589 | BAROSENSE ENDOGASTRIC TUBE (EGT), MODEL F0034 | FED | 2009-05-22 | View |
No matching devices.
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