The following data is part of a premarket notification filed by Landmark Plastics with the FDA for Cup, Disposable Medicine.
| Device ID | K760517 |
| 510k Number | K760517 |
| Device Name: | CUP, DISPOSABLE MEDICINE |
| Classification | Dispenser, Liquid Medication |
| Applicant | LANDMARK PLASTICS 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | KYX |
| CFR Regulation Number | 880.6430 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1976-08-25 |
| Decision Date | 1976-11-12 |