The following data is part of a premarket notification filed by Smith & Nephew, Mpl Division with the FDA for Micro 2 Hypodermic Needles.
| Device ID | K830242 |
| 510k Number | K830242 |
| Device Name: | MICRO 2 HYPODERMIC NEEDLES |
| Classification | Needle, Hypodermic, Single Lumen |
| Applicant | SMITH & NEPHEW, MPL DIVISION 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FMI |
| CFR Regulation Number | 880.5570 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-01-25 |
| Decision Date | 1983-02-15 |