The following data is part of a premarket notification filed by Dexide, Inc. with the FDA for Dexide Disposable Prep Stick.
| Device ID | K791168 |
| 510k Number | K791168 |
| Device Name: | DEXIDE DISPOSABLE PREP STICK |
| Classification | Applicator, Absorbent Tipped, Non-sterile |
| Applicant | DEXIDE, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KXF |
| CFR Regulation Number | 880.6025 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-06-25 |
| Decision Date | 1979-07-30 |