免责声明: 本站汇总 FDA、ClinicalTrials.gov、PubMed、SEC EDGAR 等官方公开数据，仅供一般参考，不构成医疗建议、诊断、治疗建议或投资建议。

FDA 510(k)

V-Mix

K号: K193357 · 2020-10-23

申请人Inter-Med/Vista Dental Products
决定日期2020-10-23
产品代码KJJ
决定实质等同

器械摘要

V-Mix is the device name listed in this FDA 510(k) record. The listed applicant is Inter-Med/Vista Dental Products. It received FDA 510(k) clearance on 2020-10-23 under 510(k) number K193357. The device is classified under product code KJJ. FDA Decision: Substantially Equivalent.

常见问题

What is the V-Mix?

V-Mix is a medical device that received FDA 510(k) clearance on 2020-10-23. The listed applicant is Inter-Med/Vista Dental Products. The 510(k) number is K193357.

When did V-Mix receive FDA 510(k) clearance?

V-Mix received FDA 510(k) clearance on 2020-10-23, under 510(k) number K193357.

Who is the listed applicant for V-Mix?

The FDA 510(k) record lists Inter-Med/Vista Dental Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for V-Mix?

The FDA product code for V-Mix is KJJ.

列明Inter-Med/Vista Dental Products为申报人的其他记录

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

K193409维斯塔冲洗，维斯塔冲洗加强版K193447维斯塔染料K193389维斯塔清晰K190220维斯塔FS，维斯塔FS液体K170101勇敢固化灯

相关器械（代码：KJJ）

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

K250279RC-SwiftPrepBelport Company, Inc., Gingi-PakK241354Sealer 溶剂Inter-Med, Inc.K201785EPIEN 牙科清洁剂Epien Medical, Inc.K211813特里顿Inter-Med / Vista DentalK193409维斯塔冲洗，维斯塔冲洗加强版Inter-Med/Vista Dental ProductsK200330RC-Prime 根管预备膏Pac-Dent, Inc.

官方来源

在 FDA 数据库中查看 →

数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。

↑