The following data is part of a premarket notification filed by Chesebrough-pond's U.s.a. Co. with the FDA for Chesebrough-pond's Multilayer Elastic.
| Device ID | K823852 |
| 510k Number | K823852 |
| Device Name: | CHESEBROUGH-POND'S MULTILAYER ELASTIC |
| Classification | Dressing, Wound, Drug |
| Applicant | CHESEBROUGH-POND'S U.S.A. CO. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | FRO |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-12-22 |
| Decision Date | 1983-03-17 |