Sony Medical Systems
Sony Medical Systems appears in FDA public data with 1 recall, 6 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-2771-2015, Class II) was initiated on January 13, 2015. Its most recent 510(k) clearance was granted on February 4, 2003.
Summary
- Total Recalls
- 1
- 510(k) Clearances
- 6
- Inspections
- 0
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| Z-2771-2015 | Class II | Sony LMD-1951MD, Sony LMD1951MD/BS, Sony LMD-1951MC (Foreign) 19 inch medical grade liquid crystal | January 13, 2015 |
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K024188 | UP-DF500 FILMSTATION DIGITAL FILM IMAGER | February 4, 2003 |
| K970999 | SONY PGM-100P1MD TRINITRON COLOR GRAPHIC MONITOR | May 20, 1997 |
| K961680 | SONY DKR-700 DIGITAL STILL RECORDER | July 3, 1996 |
| K931170 | SONY CARDIAC ANALYSIS AND REVIEW STATION (CARS) | June 14, 1993 |
| K924708 | CINENET CARDIAC IMAGE NETWORK | December 30, 1992 |
| K921275 | SONY LASER VIDEODISC RECORDING SYSTEM | June 10, 1992 |