REBOHIL (BGM-1, BGM-2, BGM-3, BGM-4, BGM-5)
K号: K254210 · 2026-09-25
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器械摘要
REBOHIL (BGM-1, BGM-2, BGM-3, BGM-4, BGM-5) is the device name listed in this FDA 510(k) record. The listed applicant is Hyundai Bioland Co., Ltd.. It received FDA 510(k) clearance on 2026-09-25 under 510(k) number K254210. The device is classified under product code NPM. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the REBOHIL (BGM-1, BGM-2, BGM-3, BGM-4, BGM-5)?
REBOHIL (BGM-1, BGM-2, BGM-3, BGM-4, BGM-5) is a medical device that received FDA 510(k) clearance on 2026-09-25. The listed applicant is Hyundai Bioland Co., Ltd.. The 510(k) number is K254210.
When did REBOHIL (BGM-1, BGM-2, BGM-3, BGM-4, BGM-5) receive FDA 510(k) clearance?
REBOHIL (BGM-1, BGM-2, BGM-3, BGM-4, BGM-5) received FDA 510(k) clearance on 2026-09-25, under 510(k) number K254210.
Who is the listed applicant for REBOHIL (BGM-1, BGM-2, BGM-3, BGM-4, BGM-5)?
The FDA 510(k) record lists Hyundai Bioland Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for REBOHIL (BGM-1, BGM-2, BGM-3, BGM-4, BGM-5)?
The FDA product code for REBOHIL (BGM-1, BGM-2, BGM-3, BGM-4, BGM-5) is NPM.
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。
相关器械（代码：NPM）
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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