C-beam
K号: K252735 · 2026-05-22
广告
器械摘要
C-beam is the device name listed in this FDA 510(k) record. The listed applicant is Pulmera, Inc.. It received FDA 510(k) clearance on 2026-05-22 under 510(k) number K252735. The device is classified under product code OWB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the C-beam?
C-beam is a medical device that received FDA 510(k) clearance on 2026-05-22. The listed applicant is Pulmera, Inc.. The 510(k) number is K252735.
When did C-beam receive FDA 510(k) clearance?
C-beam received FDA 510(k) clearance on 2026-05-22, under 510(k) number K252735.
Who is the listed applicant for C-beam?
The FDA 510(k) record lists Pulmera, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for C-beam?
The FDA product code for C-beam is OWB.
相关器械（代码：OWB）
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。
广告