The following data is part of a premarket notification filed by 3m Medical Products Group with the FDA for 3m No Sting Barrier Film.
| Device ID | K955103 |
| 510k Number | K955103 |
| Device Name: | 3M NO STING BARRIER FILM |
| Classification | Bandage, Liquid |
| Applicant | 3M MEDICAL PRODUCTS GROUP 3M CENTER, BLDG. 275-3E-08 St. Paul, MN 55144 -1000 |
| Contact | Anna E Mcright |
| Correspondent | Anna E Mcright 3M MEDICAL PRODUCTS GROUP 3M CENTER, BLDG. 275-3E-08 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 | 1995-11-08 |
| Decision Date | 1996-02-05 |