The following data is part of a premarket notification filed by Ets Rene Marzet with the FDA for Patient Trolley B49.
| Device ID | K792570 |
| 510k Number | K792570 |
| Device Name: | PATIENT TROLLEY B49 |
| Classification | Stretcher, Wheeled |
| Applicant | ETS RENE MARZET 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FPO |
| CFR Regulation Number | 880.6910 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-12-13 |
| Decision Date | 1979-12-31 |