Prudent 1717, Prudent 1417, Prudent 1212
K号: K211108 · 2021-06-04
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器械摘要
Prudent 1717, Prudent 1417, Prudent 1212 is the device name listed in this FDA 510(k) record. The listed applicant is Pixxgen Corporation. It received FDA 510(k) clearance on 2021-06-04 under 510(k) number K211108. The device is classified under product code MQB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Prudent 1717, Prudent 1417, Prudent 1212?
Prudent 1717, Prudent 1417, Prudent 1212 is a medical device that received FDA 510(k) clearance on 2021-06-04. The listed applicant is Pixxgen Corporation. The 510(k) number is K211108.
When did Prudent 1717, Prudent 1417, Prudent 1212 receive FDA 510(k) clearance?
Prudent 1717, Prudent 1417, Prudent 1212 received FDA 510(k) clearance on 2021-06-04, under 510(k) number K211108.
Who is the listed applicant for Prudent 1717, Prudent 1417, Prudent 1212?
The FDA 510(k) record lists Pixxgen Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Prudent 1717, Prudent 1417, Prudent 1212?
The FDA product code for Prudent 1717, Prudent 1417, Prudent 1212 is MQB.
相关临床试验
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列明Pixxgen Corporation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：MQB）
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。
K2538000909FCE，0909FCE-HSRayence Co., Ltd.K260820VIVIX-S 4386W (FXRD-4386WA)Vieworks Co., Ltd.K252996通用 1417PIKonica Minolta Healthcare Americas, Inc.K252911Lux HD 2530 探测器 (Lux HD 2530)Iray Imaging Technology (Haining) LimitedK250211玉山X射线平板探测器Innocare Optoelectronics Corp.K250665SKR 3000Konica Minolta, Inc.
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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