The following data is part of a premarket notification filed by Dms with the FDA for Restraining Stretcher.
| Device ID | K924275 |
| 510k Number | K924275 |
| Device Name: | RESTRAINING STRETCHER |
| Classification | Stretcher, Hand-carried |
| Applicant | DMS 600 S. KIWANIS Soiux Falls, SD 57104 |
| Contact | Gilber Hoogendoorm |
| Correspondent | Gilber Hoogendoorm DMS 600 S. KIWANIS Soiux Falls, SD 57104 |
| Product Code | FPP |
| CFR Regulation Number | 880.6900 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-08-25 |
| Decision Date | 1993-07-27 |