The following data is part of a premarket notification filed by Devon Industries, Inc. with the FDA for Surgical Ruler And Pen.
| Device ID | K790084 |
| 510k Number | K790084 |
| Device Name: | SURGICAL RULER AND PEN |
| Classification | Marker, Skin |
| Applicant | DEVON INDUSTRIES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FZZ |
| CFR Regulation Number | 878.4660 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-01-16 |
| Decision Date | 1979-02-26 |