The following data is part of a premarket notification filed by Ets Rene Marzet with the FDA for Obstetrical Beds.
| Device ID | K792568 |
| 510k Number | K792568 |
| Device Name: | OBSTETRICAL BEDS |
| Classification | Table, Obstetric (and Accessories) |
| Applicant | ETS RENE MARZET 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | KNC |
| CFR Regulation Number | 884.4900 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-12-13 |
| Decision Date | 1980-01-28 |