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 |