Company ยท US
Barosense, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 2009 to 2012. Name variants (Inc, Corp, punctuation) are merged.
5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Sep 10, 2012 | K120126 | BAROSENSE ENDOGASTRIC TUBE AND INTRODUCER BOUGIE Barosense, Inc. | FED |
| Feb 17, 2012 | K120147 | ACE STAPLER AND CARTRIDGE Barosense, Inc. | OCW |
| Jun 3, 2011 | K110829 | ACE STAPLER AND CARTRIDGE Barosense, Inc. | OCW |
| May 11, 2010 | K082044 | ACE STAPLER, MODEL F0031 Barosense, Inc. | OCW |
| May 22, 2009 | K082589 | BAROSENSE ENDOGASTRIC TUBE (EGT), MODEL F0034 Barosense, Inc. | FED |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||