The following data is part of a premarket notification filed by Electromed Intl., Ltd. with the FDA for View Nt.
| Device ID | K000474 |
| 510k Number | K000474 |
| Device Name: | VIEW NT |
| Classification | System, Image Processing, Radiological |
| Applicant | ELECTROMED INTL., LTD. 310 INDUSTRIAL BLVD. St-eustache, Quebec, CA J7r 5r4 |
| Contact | Pascal M Kaufmann |
| Correspondent | Pascal M Kaufmann ELECTROMED INTL., LTD. 310 INDUSTRIAL BLVD. St-eustache, Quebec, CA J7r 5r4 |
| Product Code | LLZ |
| CFR Regulation Number | 892.2050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Abbreviated |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2000-02-14 |
| Decision Date | 2000-04-19 |