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 |