The following data is part of a premarket notification filed by Chesebrough-pond's U.s.a. Co. with the FDA for Burn Pad, Dry, Sterile.
| Device ID | K781985 |
| 510k Number | K781985 |
| Device Name: | BURN PAD, DRY, STERILE |
| Classification | Gauze/sponge, Internal |
| Applicant | CHESEBROUGH-POND'S U.S.A. CO. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | EFQ |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1978-11-24 |
| Decision Date | 1978-12-07 |