The following data is part of a premarket notification filed by Johnson & Johnson Consumer Companies, Inc. with the FDA for Band-aid(r) Brand Liquid Bandage.
| Device ID | K062602 |
| 510k Number | K062602 |
| Device Name: | BAND-AID(R) BRAND LIQUID BANDAGE |
| Classification | Bandage, Liquid |
| Applicant | JOHNSON & JOHNSON CONSUMER COMPANIES, INC. 199 GRANDVIEW ROAD Skillman, NJ 08558 -9498 |
| Contact | Michelle R Turk |
| Correspondent | Michelle R Turk JOHNSON & JOHNSON CONSUMER COMPANIES, INC. 199 GRANDVIEW ROAD Skillman, NJ 08558 -9498 |
| Product Code | KMF |
| CFR Regulation Number | 880.5090 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2006-09-01 |
| Decision Date | 2006-12-11 |
| Summary: | summary |