FDA 510(k) Applications Submitted by O'CONNELL REGULATORY CONSULTANTS, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K143561 | 12/16/2014 | ELM PTA Balloon Dilatation Catheter | O'CONNELL REGULATORY CONSULTANTS, INC. |
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