The following data is part of a premarket notification filed by Benq Corporation with the FDA for Lcd Monitor (md310c, Md310g, Md210g).
| Device ID | K170944 |
| 510k Number | K170944 |
| Device Name: | LCD Monitor (MD310C, MD310G, MD210G) |
| Classification | Display, Diagnostic Radiology |
| Applicant | BenQ Corporation 16 Jihu Road, Neihu Taipei, TW 114 |
| Contact | Calvin Kt Chang |
| Correspondent | Calvin Kt Chang BenQ Corporation 16 Jihu Road, Neihu Taipei, TW 114 |
| Product Code | PGY |
| CFR Regulation Number | 892.2050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-03-30 |
| Decision Date | 2017-05-25 |
| Summary: | summary |