XO Constrain™ 经皮腔内血管成形术限制导管
K号: K232258 · 2024-06-17
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器械摘要
常见问题
What is the XO Constrain™ Percutaneous Transluminal Angioplasty Constraining Catheter?
XO Constrain™ Percutaneous Transluminal Angioplasty Constraining Catheter is a medical device that received FDA 510(k) clearance on 2024-06-17. The listed applicant is Transit Scientific, LLC. The 510(k) number is K232258.
When did XO Constrain™ Percutaneous Transluminal Angioplasty Constraining Catheter receive FDA 510(k) clearance?
XO Constrain™ Percutaneous Transluminal Angioplasty Constraining Catheter received FDA 510(k) clearance on 2024-06-17, under 510(k) number K232258.
Who is the listed applicant for XO Constrain™ Percutaneous Transluminal Angioplasty Constraining Catheter?
The FDA 510(k) record lists Transit Scientific, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for XO Constrain™ Percutaneous Transluminal Angioplasty Constraining Catheter?
The FDA product code for XO Constrain™ Percutaneous Transluminal Angioplasty Constraining Catheter is PNO.
相关临床试验
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列明Transit Scientific, LLC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：PNO）
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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