The following data is part of a premarket notification filed by Competent Design with the FDA for Tenderlift.
| Device ID | K800373 |
| 510k Number | K800373 |
| Device Name: | TENDERLIFT |
| Classification | Device, Transfer, Patient, Manual |
| Applicant | COMPETENT DESIGN 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FMR |
| CFR Regulation Number | 880.6785 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-02-20 |
| Decision Date | 1980-03-12 |