Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of SonyLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Sony Medical Systems with 6 510(k) clearances and 1 device recall. The most recent is a device recall dated Jan 13, 2015: Sony LMD-1951MD, Sony LMD1951MD/BS, Sony LMD-1951MC (Foreign) 19 inch medical grade liq….
| Jan 13, 2015 | Sony LMD-1951MD, Sony LMD1951MD/BS, Sony LMD-1951MC (Foreign) 19 inch medical grade liquid crystal display (LCD) Medical Monitors with lighClass II · Tthe medical monitor has either not turned on or has lost image during clinical use. | Device recalls |
| Feb 4, 2003 | UP-DF500 FILMSTATION DIGITAL FILM IMAGERK024188 · LMC | 510(k) clearances |
| May 20, 1997 | SONY PGM-100P1MD TRINITRON COLOR GRAPHIC MONITORK970999 · JAK | 510(k) clearances |
| Jul 3, 1996 | SONY DKR-700 DIGITAL STILL RECORDERK961680 · LMB | 510(k) clearances |
| Jun 14, 1993 | SONY CARDIAC ANALYSIS AND REVIEW STATION (CARS)K931170 · IZI | 510(k) clearances |
| Dec 30, 1992 | CINENET CARDIAC IMAGE NETWORKK924708 · IZI | 510(k) clearances |
| Jun 10, 1992 | SONY LASER VIDEODISC RECORDING SYSTEMK921275 · LMB | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
