FDA 510(k) Applications Submitted by IND NDIAGNOSTIC INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K121231 | 04/24/2012 | IND DRUG HOME MULTI-PANEL TEST (2-5) IND MORPHINE HOME TEST | IND NDIAGNOSTIC INC. |
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