The following data is part of a premarket notification filed by Edap Technomed, Inc. with the FDA for Focal One.
Device ID | K172721 |
510k Number | K172721 |
Device Name: | FOCAL ONE |
Classification | High Intensity Ultrasound System For Prostate Tissue Ablation |
Applicant | EDAP Technomed, Inc. 5321 Industrial Oaks Blvd, Suite 110 Austin, TX 78735 |
Contact | Hugo Embert |
Correspondent | Hugo Embert EDAP Technomed, Inc. 5321 Industrial Oaks Blvd, Suite 110 Austin, TX 78735 |
Product Code | PLP |
CFR Regulation Number | 876.4340 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-09-08 |
Decision Date | 2018-06-07 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
03661690000052 | K172721 | 000 |
03661690000243 | K172721 | 000 |
03661690000069 | K172721 | 000 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
FOCAL ONE 78153657 not registered Dead/Abandoned |
Novartis AG 2002-08-13 |
FOCAL ONE 78149737 not registered Dead/Abandoned |
Novartis AG 2002-08-01 |
FOCAL ONE 78127571 2764216 Dead/Cancelled |
Novartis AG 2002-05-09 |