The following data is part of a premarket notification filed by Kimberly-clark Corp. with the FDA for Kimguard One-step Sterilization Wrap.
| Device ID | K082177 |
| 510k Number | K082177 |
| Device Name: | KIMGUARD ONE-STEP STERILIZATION WRAP |
| Classification | Wrap, Sterilization |
| Applicant | KIMBERLY-CLARK CORP. 172 CONDUCTOR DRIVE Dawsonville, GA 30534 |
| Contact | Lisa Peacock |
| Correspondent | Lisa Peacock KIMBERLY-CLARK CORP. 172 CONDUCTOR DRIVE Dawsonville, GA 30534 |
| Product Code | FRG |
| CFR Regulation Number | 880.6850 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2008-08-01 |
| Decision Date | 2009-03-27 |
| Summary: | summary |