The following data is part of a premarket notification filed by Medline Industries, Lp with the FDA for Gemini Sterilization Wrap.
| Device ID | K220365 |
| 510k Number | K220365 |
| Device Name: | Gemini Sterilization Wrap |
| Classification | Wrap, Sterilization |
| Applicant | Medline Industries, LP Three Lakes Drive Northfield, IL 60093 |
| Contact | Jennifer Mason |
| Correspondent | Jennifer Mason Medline Industries, LP Three Lakes Drive Northfield, IL 60093 |
| Product Code | FRG |
| CFR Regulation Number | 880.6850 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2022-02-08 |
| Decision Date | 2022-10-06 |