The following data is part of a premarket notification filed by Exco, Inc. with the FDA for Dermafile (cat. # 38.
| Device ID | K813360 |
| 510k Number | K813360 |
| Device Name: | DERMAFILE (CAT. # 38 |
| Classification | Drape, Surgical |
| Applicant | EXCO, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KKX |
| CFR Regulation Number | 878.4370 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-11-30 |
| Decision Date | 1982-03-18 |