FDA 510(k)

数字X光摄影 CXDI-RF 无线

K号: K232298 · 2024-04-26

决定日期2024-04-26

产品代码OWB

咨询委员会RA

决定实质等同

器械摘要

DIGITAL RADIOGRAPHY CXDI-RF Wireless Bl is the device name listed in this FDA 510(k) record. The listed applicant is Canon, Inc.. It received FDA 510(k) clearance on 2024-04-26 under 510(k) number K232298. 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 DIGITAL RADIOGRAPHY CXDI-RF Wireless Bl?

DIGITAL RADIOGRAPHY CXDI-RF Wireless Bl is a medical device that received FDA 510(k) clearance on 2024-04-26. The listed applicant is Canon, Inc.. The 510(k) number is K232298.

When did DIGITAL RADIOGRAPHY CXDI-RF Wireless Bl receive FDA 510(k) clearance?

DIGITAL RADIOGRAPHY CXDI-RF Wireless Bl received FDA 510(k) clearance on 2024-04-26, under 510(k) number K232298.

Who is the listed applicant for DIGITAL RADIOGRAPHY CXDI-RF Wireless Bl?

The FDA 510(k) record lists Canon, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIGITAL RADIOGRAPHY CXDI-RF Wireless Bl?

The FDA product code for DIGITAL RADIOGRAPHY CXDI-RF Wireless Bl is OWB.

列明Canon, Inc.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。

K252503智能NR K241049CANON Fundus Camera CR-10 (CR-10)K230175Digital Radiography CXDI-CS01 K222855数字放射摄影CXDI-Pro，数字放射摄影D1 K222687数字放射摄影CXDI-Elite，数字放射摄影E1 K222661数字放射摄影CXDI-CS01

查看所有 24 个设备 →

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。