Company ยท US
Smith & Nephew, Mpl Division
FDA 510(k) clearances and medical device recalls filed under this name, 1976 to 1984. Name variants (Inc, Corp, punctuation) are merged.
9510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Sep 27, 1984 | K843314 | MPL HYPO BRAND BREECH LOAD ASPIR SYRINGE Smith & Nephew, Mpl Division | EJI |
| May 21, 1984 | K841280 | SOLOPAK BRAND FILTER NEEDLE W/5 MICRO Smith & Nephew, Mpl Division | FPB |
| Apr 5, 1984 | K840237 | MAX-I-PROBE PERIODONTAL ENDODONTIC PROB Smith & Nephew, Mpl Division | EIC |
| Mar 30, 1984 | K833304 | HYPO BRAND DISPOS. DENTAL NEEDLES-PLAST Smith & Nephew, Mpl Division | DZM |
| Aug 12, 1983 | K832126 | MICRO Z DISPOS. SPINAL ANESTH. NEEDLE Smith & Nephew, Mpl Division | BSP |
| Jul 12, 1983 | K831765 | HERAPIN LOCK FLUSH SOLUTION USE KIT Smith & Nephew, Mpl Division | FMI |
| Mar 24, 1983 | K830524 | HENKE JECT PRESSURE SYRINGE Smith & Nephew, Mpl Division | EJI |
| Feb 15, 1983 | K830242 | MICRO 2 HYPODERMIC NEEDLES Smith & Nephew, Mpl Division | FMI |
| Dec 13, 1976 | K761206 | INTEROSSEOUS NEEDLE Smith & Nephew, Mpl Division | DZM |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||