The following data is part of a premarket notification filed by Lancer Assoc. with the FDA for Tender Lifting Care.
| Device ID | K840796 |
| 510k Number | K840796 |
| Device Name: | TENDER LIFTING CARE |
| Classification | Device, Patient Transfer, Powered |
| Applicant | LANCER ASSOC. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | FRZ |
| CFR Regulation Number | 880.6775 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-02-23 |
| Decision Date | 1984-04-20 |