K973039 is an FDA 510(k) clearance for the LEGACY/LEGACY-D TABLE. This device is classified as a Table, Radiographic, Tilting (Class II - Special Controls, product code IXR).
Submitted by GE Medical Systems (Milwaukee, US). The FDA issued a Cleared decision on October 16, 1997, 63 days after receiving the submission on August 14, 1997.
This device falls under the Radiology FDA review panel. Regulated under 21 CFR 892.1980.
| 510(k) Number | K973039 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | August 14, 1997 |
| Decision Date | October 16, 1997 |
| Days to Decision | 63 days |
| Submission Type | Traditional |
| Review Panel | Radiology (RA) |
| Summary | Summary PDF |
| Product Code | IXR - Table, Radiographic, Tilting |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 892.1980 |