Vista FS, Vista FS Liquid
FDA 510(k) clearance K190220 · decided 2019-06-10
Clearance details
- K-number
- K190220
- Device name
- Vista FS, Vista FS Liquid
- Applicant
- Inter-Med/Vista Dental Products
- Decision
- Substantially Equivalent
- Date received
- 2019-02-05
- Decision date
- 2019-06-10
- Days to decision
- 125 days
- Clearance type
- Traditional
- Product code
- MVL
- Device class
- U
- Medical specialty
- Unknown
- Advisory committee
- Unknown
- Location
- Racine, WI, US
- Third-party review
- No
- Expedited review
- No
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|---|---|---|
| Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit, Catalog number 504600-28 recall (Z-2400-2026) | Inter-Med Llc | 2026-06-10 |