The following data is part of a premarket notification filed by Kaycor Intl., Ltd. with the FDA for Yoshida Ap 100.
| Device ID | K811211 |
| 510k Number | K811211 |
| Device Name: | YOSHIDA AP 100 |
| Classification | Processor, Radiographic-film, Automatic, Dental |
| Applicant | KAYCOR INTL., LTD. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | EGY |
| CFR Regulation Number | 892.1900 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-05-04 |
| Decision Date | 1981-06-16 |