The following data is part of a premarket notification filed by Orthopedic Equipment Co., Inc. with the FDA for Patient Lift.
| Device ID | K780684 |
| 510k Number | K780684 |
| Device Name: | PATIENT LIFT |
| Classification | Lift, Patient, Non-ac-powered |
| Applicant | ORTHOPEDIC EQUIPMENT CO., INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FSA |
| CFR Regulation Number | 880.5510 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1978-04-24 |
| Decision Date | 1978-06-06 |