The following data is part of a premarket notification filed by Sonomed, Inc. with the FDA for Master-vu.
| Device ID | K073196 |
| 510k Number | K073196 |
| Device Name: | MASTER-VU |
| Classification | System, Imaging, Pulsed Echo, Ultrasonic |
| Applicant | SONOMED, INC. 377 ROUTE 17 S Hasbrouck Heights, NJ 07604 |
| Contact | George Myers |
| Correspondent | George Myers SONOMED, INC. 377 ROUTE 17 S Hasbrouck Heights, NJ 07604 |
| Product Code | IYO |
| CFR Regulation Number | 892.1560 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2007-11-13 |
| Decision Date | 2007-12-19 |
| Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() MASTER-VU 77135599 3485737 Dead/Cancelled |
Sonomed, Inc. 2007-03-20 |