The following data is part of a premarket notification filed by 3m Company with the FDA for 3m Steri-strip Antimicrobial Skin Clos.
| Device ID | K813265 |
| 510k Number | K813265 |
| Device Name: | 3M STERI-STRIP ANTIMICROBIAL SKIN CLOS |
| Classification | Tape And Bandage, Adhesive |
| Applicant | 3M COMPANY 8124 PACIFIC AVE. White City, OR 97503 |
| Product Code | KGX |
| CFR Regulation Number | 880.5240 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-11-20 |
| Decision Date | 1983-02-09 |