The following data is part of a premarket notification filed by Johnson & Johnson Consumer Products, Inc. with the FDA for Johnson & Johnson Easy Slide Dental Floss.
| Device ID | K951917 |
| 510k Number | K951917 |
| Device Name: | JOHNSON & JOHNSON EASY SLIDE DENTAL FLOSS |
| Classification | Floss, Dental |
| Applicant | JOHNSON & JOHNSON CONSUMER PRODUCTS, INC. 199 GRANDVIEW RD. Skillman, NJ 08558 -9418 |
| Contact | Diana L B. Uhl |
| Correspondent | Diana L B. Uhl JOHNSON & JOHNSON CONSUMER PRODUCTS, INC. 199 GRANDVIEW RD. Skillman, NJ 08558 -9418 |
| Product Code | JES |
| CFR Regulation Number | 872.6390 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-04-24 |
| Decision Date | 1995-05-10 |