FDA 510(k) Applications Submitted by COMMON SENSE, LTD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K071100 | 04/19/2007 | AMNISCREEN HOME DETECTION LINER KIT | COMMON SENSE, LTD. |
| K091287 | 05/01/2009 | VS-SENSE TEST | COMMON SENSE, LTD. |
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