510(k) K190220 ยท MVL Cord, Retraction
Vista FS, Vista FS Liquid
| Applicant | Inter-Med/Vista Dental Products, Racine WI, US |
| Decision | Substantially Equivalent, Jun 10, 2019 |
| Received | Feb 5, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K190220
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jun 10, 2026 | Inter-Med Llc Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit,
Catalog number 504600-28 Open, Classified |
MVL | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.