FDA 510(k) Applications Submitted by REGENESIS BIOMEDICAL, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K091791 | 06/17/2009 | PROVANT SYSTEM, MODEL 4201 | REGENESIS BIOMEDICAL, INC. |
| K131979 | 06/28/2013 | PROVANT THERAPY SYSTEM | REGENESIS BIOMEDICAL, INC. |
| K972093 | 06/04/1997 | REGENESIS MODEL 42 | REGENESIS BIOMEDICAL, INC. |
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