FDA 510(k) Applications Submitted by AMERICAN I.V. PRODUCTS, INC dba AIV, INC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K142333 | 08/21/2014 | SMART LABEL, PROPOFOL | AMERICAN I.V. PRODUCTS, INC dba AIV, INC |
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