The following data is part of a premarket notification filed by Landmark Plastics with the FDA for Cup, Disposable Specimen.
| Device ID | K760496 |
| 510k Number | K760496 |
| Device Name: | CUP, DISPOSABLE SPECIMEN |
| Classification | Container, Specimen, Sterile |
| Applicant | LANDMARK PLASTICS 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FMH |
| CFR Regulation Number | 864.3250 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1976-08-23 |
| Decision Date | 1976-11-12 |