The following data is part of a premarket notification filed by Vucomp, Inc. with the FDA for M-vu Viewer Station.
| Device ID | K060451 |
| 510k Number | K060451 |
| Device Name: | M-VU VIEWER STATION |
| Classification | System, Image Processing, Radiological |
| Applicant | VUCOMP, INC. 55 Northern Blvd. Suite 200 Great Neck, NY 11021 |
| Contact | Susan D Goldstein-falk |
| Correspondent | Susan D Goldstein-falk VUCOMP, INC. 55 Northern Blvd. Suite 200 Great Neck, NY 11021 |
| Product Code | LLZ |
| CFR Regulation Number | 892.2050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2006-02-21 |
| Decision Date | 2006-03-22 |
| Summary: | summary |