The following data is part of a premarket notification filed by Medical Products Manufacturing, Inc. with the FDA for Sonomark.
Device ID | K061560 |
510k Number | K061560 |
Device Name: | SONOMARK |
Classification | Transducer, Ultrasonic, Diagnostic |
Applicant | MEDICAL PRODUCTS MANUFACTURING, INC. 11495-3800 ROAD Paonia, CO 81428 |
Contact | Theron E Johnson |
Correspondent | Theron E Johnson MEDICAL PRODUCTS MANUFACTURING, INC. 11495-3800 ROAD Paonia, CO 81428 |
Product Code | ITX |
CFR Regulation Number | 892.1570 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2006-06-05 |
Decision Date | 2006-08-18 |
Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SONOMARK 87072513 5128392 Live/Registered |
Huff, Blane 2016-06-15 |
SONOMARK 78792138 3486326 Dead/Cancelled |
Medical Products Manufacturing, Inc. 2006-01-16 |
SONOMARK 74348925 1832193 Dead/Cancelled |
Sonoco Products Company 1993-01-15 |