The following data is part of a premarket notification filed by Beiersdorf, Inc. with the FDA for Cutinova(r) Plus Foam Gelfilm.
| Device ID | K864913 |
| 510k Number | K864913 |
| Device Name: | CUTINOVA(R) PLUS FOAM GELFILM |
| Classification | Dressing, Wound, Drug |
| Applicant | BEIERSDORF, INC. 360 MARTIN LUTHER KING DR. P.O. BOX 5529 Norwalk, CT 06856 |
| Contact | Vincent Milano |
| Correspondent | Vincent Milano BEIERSDORF, INC. 360 MARTIN LUTHER KING DR. P.O. BOX 5529 Norwalk, CT 06856 |
| Product Code | FRO |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent For Some Indications (SN) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1986-12-16 |
| Decision Date | 1987-07-24 |