The following data is part of a premarket notification filed by Wipak Oy with the FDA for Steiking Packaging For Medical Devices.
| Device ID | K210810 |
| 510k Number | K210810 |
| Device Name: | Steiking Packaging For Medical Devices |
| Classification | Wrap, Sterilization |
| Applicant | Wipak OY Wipaktie 2 Nastola, FI Fi-15560 |
| Contact | Mira Santala |
| Correspondent | Steven T. Singleton Compliance Systems International LLC. 7 Windham Hill Mendon, NY 14056 |
| Product Code | FRG |
| CFR Regulation Number | 880.6850 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2021-03-17 |
| Decision Date | 2022-01-23 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 06438263665713 | K210810 | 000 |
| 06438263667274 | K210810 | 000 |
| 06438263667281 | K210810 | 000 |
| 06438263667250 | K210810 | 000 |
| 06438263666505 | K210810 | 000 |
| 06438264180024 | K210810 | 000 |
| 06438264180031 | K210810 | 000 |
| 06438264180055 | K210810 | 000 |
| 06438264180062 | K210810 | 000 |
| 06438263665584 | K210810 | 000 |
| 06438263667267 | K210810 | 000 |