FDA 510(k) Applications Submitted by CAIRE, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K120785 | 03/15/2012 | OMNI 3 OXYGEN SYSTEM | CAIRE, INC. |
| K050153 | 01/24/2005 | SPIRIT, MODEL HAS | CAIRE, INC. |
| K013251 | 09/28/2001 | SPIRIT 300 | CAIRE, INC. |
| K080023 | 01/04/2008 | MODIFICATION TO: SPIRIT | CAIRE, INC. |
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