Smith & Nephew, Mpl Division
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 9
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K843314 | MPL HYPO BRAND BREECH LOAD ASPIR SYRINGE | September 27, 1984 |
| K841280 | SOLOPAK BRAND FILTER NEEDLE W/5 MICRO | May 21, 1984 |
| K840237 | MAX-I-PROBE PERIODONTAL ENDODONTIC PROB | April 5, 1984 |
| K833304 | HYPO BRAND DISPOS. DENTAL NEEDLES-PLAST | March 30, 1984 |
| K832126 | MICRO Z DISPOS. SPINAL ANESTH. NEEDLE | August 12, 1983 |
| K831765 | HERAPIN LOCK FLUSH SOLUTION USE KIT | July 12, 1983 |
| K830524 | HENKE JECT PRESSURE SYRINGE | March 24, 1983 |
| K830242 | MICRO 2 HYPODERMIC NEEDLES | February 15, 1983 |
| K761206 | INTEROSSEOUS NEEDLE | December 13, 1976 |