Smith & Nephew, Mpl Division
FDA 510(k) & PMA Approved Devices — 9 products
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Total Devices9
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K843314 | MPL HYPO BRAND BREECH LOAD ASPIR SYRINGE | EJI | 1984-09-27 | View |
| 510(k) | K841280 | SOLOPAK BRAND FILTER NEEDLE W/5 MICRO | FPB | 1984-05-21 | View |
| 510(k) | K840237 | MAX-I-PROBE PERIODONTAL ENDODONTIC PROB | EIC | 1984-04-05 | View |
| 510(k) | K833304 | HYPO BRAND DISPOS. DENTAL NEEDLES-PLAST | DZM | 1984-03-30 | View |
| 510(k) | K832126 | MICRO Z DISPOS. SPINAL ANESTH. NEEDLE | BSP | 1983-08-12 | View |
| 510(k) | K831765 | HERAPIN LOCK FLUSH SOLUTION USE KIT | FMI | 1983-07-12 | View |
| 510(k) | K830524 | HENKE JECT PRESSURE SYRINGE | EJI | 1983-03-24 | View |
| 510(k) | K830242 | MICRO 2 HYPODERMIC NEEDLES | FMI | 1983-02-15 | View |
| 510(k) | K761206 | INTEROSSEOUS NEEDLE | DZM | 1976-12-13 | View |
No matching devices.
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