The following data is part of a premarket notification filed by 3m Company with the FDA for 3m Liquid Bandage, Model 120-lb.
| Device ID | K031263 |
| 510k Number | K031263 |
| Device Name: | 3M LIQUID BANDAGE, MODEL 120-LB |
| Classification | Bandage, Liquid |
| Applicant | 3M COMPANY 3M CENTER, BLDG. 275-5W-06 St. Paul, MN 55133 -3275 |
| Contact | Anna E Mcright |
| Correspondent | Anna E Mcright 3M COMPANY 3M CENTER, BLDG. 275-5W-06 St. Paul, MN 55133 -3275 |
| Product Code | KMF |
| CFR Regulation Number | 880.5090 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2003-04-21 |
| Decision Date | 2003-10-07 |
| Summary: | summary |