The following data is part of a premarket notification filed by Landmark Plastics with the FDA for Bedpan, General Medical Medi-pak.
| Device ID | K760490 |
| 510k Number | K760490 |
| Device Name: | BEDPAN, GENERAL MEDICAL MEDI-PAK |
| Classification | Bedpan |
| Applicant | LANDMARK PLASTICS 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FOB |
| CFR Regulation Number | 880.6730 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1976-08-23 |
| Decision Date | 1976-11-12 |