The following data is part of a premarket notification filed by Sony Electronics, Inc. with the FDA for Sony Lmd-2451mt Lcd Monitor.
| Device ID | K113203 |
| 510k Number | K113203 |
| Device Name: | SONY LMD-2451MT LCD MONITOR |
| Classification | Laparoscope, General & Plastic Surgery |
| Applicant | SONY ELECTRONICS, INC. 49 PLAIN STREET North Attleboro, MA 02760 |
| Contact | Cynthia Sinclair |
| Correspondent | Cynthia Sinclair SONY ELECTRONICS, INC. 49 PLAIN STREET North Attleboro, MA 02760 |
| Product Code | GCJ |
| CFR Regulation Number | 876.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2011-10-31 |
| Decision Date | 2012-02-24 |
| Summary: | summary |