Teleflexmedical, Inc. · Class II · Cleared May 8, 2019
| K-number | K183461 |
| Device name | Rusch Flocath Hydrophilic Intermittent Catheter, Rusch MMG Hydrophilic Intermittent Catheter |
| Applicant | Teleflexmedical, Inc. |
| Product code | GBM |
| Device class | Class II |
| Decision date | May 8, 2019 |
| Decision | Unknown |
| Regulation | 876.5130 |
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