The following data is part of a premarket notification filed by Henry Enterprises, Inc. with the FDA for Lift Master Patient Lift.
| Device ID | K896848 |
| 510k Number | K896848 |
| Device Name: | LIFT MASTER PATIENT LIFT |
| Classification | Lift, Patient, Ac-powered |
| Applicant | HENRY ENTERPRISES, INC. P.O. BOX 24 Concordia, KS 66901 |
| Contact | Barbara J Henry |
| Correspondent | Barbara J Henry HENRY ENTERPRISES, INC. P.O. BOX 24 Concordia, KS 66901 |
| Product Code | FNG |
| CFR Regulation Number | 880.5500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-12-05 |
| Decision Date | 1990-05-29 |