FDA 510(k)

ScandiDos Delta4 Discover，备选商品名称：ScandiDos Delta4 Discover+

K号: K151426 · 2016-01-29

决定日期2016-01-29

产品代码IYE

咨询委员会RA

决定实质等同

器械摘要

ScandiDos Delta4 Discover, Alternative Trade Name: ScandiDos Delta4 Discover+ is the device name listed in this FDA 510(k) record. The listed applicant is Scandidos AB. It received FDA 510(k) clearance on 2016-01-29 under 510(k) number K151426. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the ScandiDos Delta4 Discover, Alternative Trade Name: ScandiDos Delta4 Discover+?

ScandiDos Delta4 Discover, Alternative Trade Name: ScandiDos Delta4 Discover+ is a medical device that received FDA 510(k) clearance on 2016-01-29. The listed applicant is Scandidos AB. The 510(k) number is K151426.

When did ScandiDos Delta4 Discover, Alternative Trade Name: ScandiDos Delta4 Discover+ receive FDA 510(k) clearance?

ScandiDos Delta4 Discover, Alternative Trade Name: ScandiDos Delta4 Discover+ received FDA 510(k) clearance on 2016-01-29, under 510(k) number K151426.

Who is the listed applicant for ScandiDos Delta4 Discover, Alternative Trade Name: ScandiDos Delta4 Discover+?

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

What is the FDA product code for ScandiDos Delta4 Discover, Alternative Trade Name: ScandiDos Delta4 Discover+?

The FDA product code for ScandiDos Delta4 Discover, Alternative Trade Name: ScandiDos Delta4 Discover+ is IYE.

列明Scandidos AB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。

K223234Delta4 Insight K183606Delta4 Phantom+ MR (PMMA), Delta4 Phantom+ MR (PW)

官方来源

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