The following data is part of a premarket notification filed by Inter-med / Vista Dental Products with the FDA for Vista Fs, Vista Fs Liquid.
| Device ID | K190220 |
| 510k Number | K190220 |
| Device Name: | Vista FS, Vista FS Liquid |
| Classification | Cord, Retraction |
| Applicant | Inter-Med / Vista Dental Products 2200 South St. Ste. A Racine, WI 53404 |
| Contact | Alex Johnson |
| Correspondent | Alex Johnson Inter-Med / Vista Dental Products 2200 South St. Ste. A Racine, WI 53404 |
| Product Code | MVL |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2019-02-05 |
| Decision Date | 2019-06-10 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 20818207020516 | K190220 | 000 |
| 00818207020529 | K190220 | 000 |
| 20304040151444 | K190220 | 000 |
| 10304040151430 | K190220 | 000 |
| 10304040151423 | K190220 | 000 |
| 10304040151409 | K190220 | 000 |
| 10304040151393 | K190220 | 000 |
| 10304040151379 | K190220 | 000 |
| 20304040151413 | K190220 | 000 |