The following data is part of a premarket notification filed by Tri W-g, Inc. with the FDA for Powered Patient System.
| Device ID | K810220 |
| 510k Number | K810220 |
| Device Name: | POWERED PATIENT SYSTEM |
| Classification | Bed, Patient Rotation, Powered |
| Applicant | TRI W-G, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | IKZ |
| CFR Regulation Number | 890.5225 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-01-27 |
| Decision Date | 1981-02-04 |