FDA 510(k) Applications Submitted by CHEST M.I., INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K080921 | 04/01/2008 | SPIRO-MASTER PC-10 SPIROMETRY SYSTEM | CHEST M.I., INC. |
| K090646 | 03/11/2009 | CARDIOTECH SPIROMETRY SYSTEM, MODEL GT-105 | CHEST M.I., INC. |
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