The following data is part of a premarket notification filed by Topcon Medical Systems, Inc. with the FDA for Trc-nw300 Non-mydriatic Retinal Camera.
| Device ID | K123460 |
| 510k Number | K123460 |
| Device Name: | TRC-NW300 NON-MYDRIATIC RETINAL CAMERA |
| Classification | Camera, Ophthalmic, Ac-powered |
| Applicant | TOPCON MEDICAL SYSTEMS, INC. 111 BAUER DR Oakland, NJ 07436 |
| Contact | Michael Gusel |
| Correspondent | Michael Gusel TOPCON MEDICAL SYSTEMS, INC. 111 BAUER DR Oakland, NJ 07436 |
| Product Code | HKI |
| CFR Regulation Number | 886.1120 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-11-09 |
| Decision Date | 2013-02-06 |
| Summary: | summary |