FDA 510(k)

Avazzia OTC TENS for aesthetics, model BEST-AV1®: EZZI-LIFT® Device

K号: K191951 · 2021-04-27

决定日期2021-04-27

产品代码NFO

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决定实质等同

器械摘要

Avazzia OTC TENS for aesthetics, model BEST-AV1™: EZZI-LIFT™ Device is the device name listed in this FDA 510(k) record. The listed applicant is Avazzia, Inc.. It received FDA 510(k) clearance on 2021-04-27 under 510(k) number K191951. The device is classified under product code NFO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Avazzia OTC TENS for aesthetics, model BEST-AV1™: EZZI-LIFT™ Device?

Avazzia OTC TENS for aesthetics, model BEST-AV1™: EZZI-LIFT™ Device is a medical device that received FDA 510(k) clearance on 2021-04-27. The listed applicant is Avazzia, Inc.. The 510(k) number is K191951.

When did Avazzia OTC TENS for aesthetics, model BEST-AV1™: EZZI-LIFT™ Device receive FDA 510(k) clearance?

Avazzia OTC TENS for aesthetics, model BEST-AV1™: EZZI-LIFT™ Device received FDA 510(k) clearance on 2021-04-27, under 510(k) number K191951.

Who is the listed applicant for Avazzia OTC TENS for aesthetics, model BEST-AV1™: EZZI-LIFT™ Device?

The FDA 510(k) record lists Avazzia, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Avazzia OTC TENS for aesthetics, model BEST-AV1™: EZZI-LIFT™ Device?

The FDA product code for Avazzia OTC TENS for aesthetics, model BEST-AV1™: EZZI-LIFT™ Device is NFO.

列明Avazzia, Inc.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。

K162392Avazzia

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