Portex, Inc. · Class II · Cleared Feb 13, 2002
| K-number | K014073 |
| Device name | HYPODERMIC NEEDLE-PRO INSULIN SYRINE & NEEDLE WITH NEEDLE PROTECTION DEVICE |
| Applicant | Portex, Inc. |
| Product code | FMF |
| Device class | Class II |
| Decision date | Feb 13, 2002 |
| Decision | Substantially Equivalent |
| Regulation | 880.5860 |
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