The following data is part of a premarket notification filed by Dermatec, Inc. with the FDA for Dermatex Sterile Finger Bandage.
| Device ID | K833638 |
| 510k Number | K833638 |
| Device Name: | DERMATEX STERILE FINGER BANDAGE |
| Classification | Dressing, Wound, Drug |
| Applicant | DERMATEC, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| 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 | 1983-10-17 |
| Decision Date | 1983-12-27 |