The following data is part of a premarket notification filed by Jeffrey Ward Cash, Dds with the FDA for Voutia™.
Device ID | K173808 |
510k Number | K173808 |
Device Name: | Voutia™ |
Classification | Saliva, Artificial |
Applicant | Jeffrey Ward Cash, DDS 10149 Bon Air Crest Drive North Chesterfield, VA 23235 -4868 |
Contact | Jeffrey Ward Cash |
Correspondent | Jeffrey Ward Cash Jeffrey Ward Cash, DDS 10149 Bon Air Crest Drive North Chesterfield, VA 23235 -4868 |
Product Code | LFD |
CFR Regulation Number | 510(k) Premarket Notification [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-12-15 |
Decision Date | 2018-07-27 |
Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
VOUTIA 87393736 5456753 Live/Registered |
Cash, Jeffrey Ward 2017-03-31 |