FDA 510(k) Applications Submitted by ALERE SAN DIEGO, INC (FORMALLY BIOSITE INCORPORATE
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K110212 | 01/25/2011 | INRATIO2 PI/NR MONITORING SYSTEM; INRATIO PT/INR TEST STRIP | ALERE SAN DIEGO, INC (FORMALLY BIOSITE INCORPORATE |
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