The following data is part of a premarket notification filed by Sony Medical Electronics Co. with the FDA for Sony Trinitron Color Video Monitor Pvm-1343md.
| Device ID | K885042 |
| 510k Number | K885042 |
| Device Name: | SONY TRINITRON COLOR VIDEO MONITOR PVM-1343MD |
| Classification | Camera, Surgical And Accessories |
| Applicant | SONY MEDICAL ELECTRONICS CO. 45 WEST ST. SUITE 2 Attleboro, MA 02703 |
| Contact | Cynthia A Sinclair |
| Correspondent | Cynthia A Sinclair SONY MEDICAL ELECTRONICS CO. 45 WEST ST. SUITE 2 Attleboro, MA 02703 |
| Product Code | KQM |
| CFR Regulation Number | 878.4160 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-12-05 |
| Decision Date | 1988-12-22 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 04548736111684 | K885042 | 000 |
| 04548736111677 | K885042 | 000 |