The following data is part of a premarket notification filed by Devine Medical Products with the FDA for Ltdt Patient Lifter.
| Device ID | K884110 |
| 510k Number | K884110 |
| Device Name: | LTDT PATIENT LIFTER |
| Classification | Transport, Patient, Powered |
| Applicant | DEVINE MEDICAL PRODUCTS 11677 HILL RD. Marysville, CA 95901 |
| Contact | Gary Schaal |
| Correspondent | Gary Schaal DEVINE MEDICAL PRODUCTS 11677 HILL RD. Marysville, CA 95901 |
| Product Code | ILK |
| CFR Regulation Number | 890.5150 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-09-29 |
| Decision Date | 1988-10-13 |