FDA 510(k) Applications Submitted by IRIS DIAGNOSTICS
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K072640 | 09/18/2007 | IRISPEC,CA/CB/CC | IRIS DIAGNOSTICS |
| K091539 | 05/26/2009 | IQ 200 URINE ANALIZER BODY FLUIDS MODULE | IRIS DIAGNOSTICS |
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