MucoPEG
K号: K190144 · 2019-11-05
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器械摘要
MucoPEG is the device name listed in this FDA 510(k) record. The listed applicant is Sunbio, Inc.. It received FDA 510(k) clearance on 2019-11-05 under 510(k) number K190144. The device is classified under product code LFD. FDA Decision: Substantially Equivalent.
常见问题
What is the MucoPEG?
MucoPEG is a medical device that received FDA 510(k) clearance on 2019-11-05. The listed applicant is Sunbio, Inc.. The 510(k) number is K190144.
When did MucoPEG receive FDA 510(k) clearance?
MucoPEG received FDA 510(k) clearance on 2019-11-05, under 510(k) number K190144.
Who is the listed applicant for MucoPEG?
The FDA 510(k) record lists Sunbio, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MucoPEG?
The FDA product code for MucoPEG is LFD.
相关临床试验
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相关器械（代码：LFD）
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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