The following data is part of a premarket notification filed by S. Jackson, Inc. with the FDA for Jackson Hydro System.
| Device ID | K802780 |
| 510k Number | K802780 |
| Device Name: | JACKSON HYDRO SYSTEM |
| Classification | Lift, Patient, Ac-powered |
| Applicant | S. JACKSON, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FNG |
| CFR Regulation Number | 880.5500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-11-05 |
| Decision Date | 1980-12-10 |