The following data is part of a premarket notification filed by Dutton-lainson Co. with the FDA for Sanitas Patient Lift.
| Device ID | K930625 |
| 510k Number | K930625 |
| Device Name: | SANITAS PATIENT LIFT |
| Classification | Lift, Patient, Non-ac-powered |
| Applicant | DUTTON-LAINSON CO. 451 WEST SECOND ST. Hastings, NE 68902 |
| Contact | Ron Haase |
| Correspondent | Ron Haase DUTTON-LAINSON CO. 451 WEST SECOND ST. Hastings, NE 68902 |
| Product Code | FSA |
| CFR Regulation Number | 880.5510 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-02-08 |
| Decision Date | 1993-09-13 |