The following data is part of a premarket notification filed by Taylor Medical Equipment with the FDA for Taylor Patient Transfer Board.
| Device ID | K792247 |
| 510k Number | K792247 |
| Device Name: | TAYLOR PATIENT TRANSFER BOARD |
| Classification | Aid, Transfer |
| Applicant | TAYLOR MEDICAL EQUIPMENT 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | IKX |
| CFR Regulation Number | 890.5050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-11-07 |
| Decision Date | 1979-11-30 |