The following data is part of a premarket notification filed by Ge Medical Systems with the FDA for Legacy/legacy-d Table.
| Device ID | K973039 |
| 510k Number | K973039 |
| Device Name: | LEGACY/LEGACY-D TABLE |
| Classification | Table, Radiographic, Tilting |
| Applicant | GE MEDICAL SYSTEMS P.O. BOX 414 Milwaukee, WI 53201 |
| Contact | Larry A Kroger |
| Correspondent | Larry A Kroger GE MEDICAL SYSTEMS P.O. BOX 414 Milwaukee, WI 53201 |
| Product Code | IXR |
| CFR Regulation Number | 892.1980 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1997-08-14 |
| Decision Date | 1997-10-16 |
| Summary: | summary |