The following data is part of a premarket notification filed by 3m Company with the FDA for 3m Liquid Bandage.
| Device ID | K053409 |
| 510k Number | K053409 |
| Device Name: | 3M LIQUID BANDAGE |
| Classification | Bandage, Liquid |
| Applicant | 3M COMPANY 3M CENTER, BLDG. 275-5W-06 St. Paul, MN 55144 -1000 |
| Contact | Bryan Becker |
| Correspondent | Bryan Becker 3M COMPANY 3M CENTER, BLDG. 275-5W-06 St. Paul, MN 55144 -1000 |
| Product Code | KMF |
| CFR Regulation Number | 880.5090 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2005-12-07 |
| Decision Date | 2006-06-19 |
| Summary: | summary |