The following data is part of a premarket notification filed by Ypsomed Ag with the FDA for Clickfine Pen Needle.
| Device ID | K102108 |
| 510k Number | K102108 |
| Device Name: | CLICKFINE PEN NEEDLE |
| Classification | Needle, Hypodermic, Single Lumen |
| Applicant | YPSOMED AG BRUNNMATTSTRASSE 6 Burgdorf, CH Ch-3401 |
| Contact | Manfred Mader |
| Correspondent | Manfred Mader YPSOMED AG BRUNNMATTSTRASSE 6 Burgdorf, CH Ch-3401 |
| Product Code | FMI |
| CFR Regulation Number | 880.5570 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2010-07-27 |
| Decision Date | 2010-11-23 |
| Summary: | summary |