Bonvadis 乳膏
K号: K212554 · 2022-08-19
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器械摘要
Bonvadis Topical Cream is the device name listed in this FDA 510(k) record. The listed applicant is Stemcyte, Inc.. It received FDA 510(k) clearance on 2022-08-19 under 510(k) number K212554. The device is classified under product code FRO. Product code FRO falls under the category of Anesthesiology, which includes devices for anesthetic delivery and patient monitoring. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.
常见问题
What is the Bonvadis Topical Cream?
Bonvadis Topical Cream is a medical device that received FDA 510(k) clearance on 2022-08-19. The listed applicant is Stemcyte, Inc.. The 510(k) number is K212554.
When did Bonvadis Topical Cream receive FDA 510(k) clearance?
Bonvadis Topical Cream received FDA 510(k) clearance on 2022-08-19, under 510(k) number K212554.
Who is the listed applicant for Bonvadis Topical Cream?
The FDA 510(k) record lists Stemcyte, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Bonvadis Topical Cream?
The FDA product code for Bonvadis Topical Cream is FRO. This falls under the Anesthesiology category.
相关临床试验
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列明Stemcyte, 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。
相关器械（代码：FRO）
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。
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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。
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