一次性医疗设备自封灭菌袋,一次性医疗设备灭菌卷袋
K号: K193561 · 2020-04-15
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器械摘要
常见问题
What is the Diposable Medical Device Self-seal Sterilization Pouch, Disposable Medical Device Sterilization Reel Pouch?
Diposable Medical Device Self-seal Sterilization Pouch, Disposable Medical Device Sterilization Reel Pouch is a medical device that received FDA 510(k) clearance on 2020-04-15. The listed applicant is Weihai Xingtai Packaging Products Co., Ltd.. The 510(k) number is K193561.
When did Diposable Medical Device Self-seal Sterilization Pouch, Disposable Medical Device Sterilization Reel Pouch receive FDA 510(k) clearance?
Diposable Medical Device Self-seal Sterilization Pouch, Disposable Medical Device Sterilization Reel Pouch received FDA 510(k) clearance on 2020-04-15, under 510(k) number K193561.
Who is the listed applicant for Diposable Medical Device Self-seal Sterilization Pouch, Disposable Medical Device Sterilization Reel Pouch?
The FDA 510(k) record lists Weihai Xingtai Packaging Products Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Diposable Medical Device Self-seal Sterilization Pouch, Disposable Medical Device Sterilization Reel Pouch?
The FDA product code for Diposable Medical Device Self-seal Sterilization Pouch, Disposable Medical Device Sterilization Reel Pouch is FRG.
相关临床试验
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。
列明Weihai Xingtai Packaging Products Co., Ltd.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:FRG)
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。
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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