FDA 510(k) Applications Submitted by HOLLISTER, INCORPORATED
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K110862 | 03/29/2011 | VAPRO PLUS INTERMITTENT CATHETER | HOLLISTER, INCORPORATED |
| K141642 | 06/19/2014 | VAPRO INTERMITTENT CATHETER | HOLLISTER, INCORPORATED |
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