CFP-3131，CFP-2222
K号: K201172 · 2020-05-29
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器械摘要
CFP-3131, CFP-2222 is the device name listed in this FDA 510(k) record. The listed applicant is Mx Imaging, Inc.. It received FDA 510(k) clearance on 2020-05-29 under 510(k) number K201172. 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 CFP-3131, CFP-2222?
CFP-3131, CFP-2222 is a medical device that received FDA 510(k) clearance on 2020-05-29. The listed applicant is Mx Imaging, Inc.. The 510(k) number is K201172.
When did CFP-3131, CFP-2222 receive FDA 510(k) clearance?
CFP-3131, CFP-2222 received FDA 510(k) clearance on 2020-05-29, under 510(k) number K201172.
Who is the listed applicant for CFP-3131, CFP-2222?
The FDA 510(k) record lists Mx Imaging, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CFP-3131, CFP-2222?
The FDA product code for CFP-3131, CFP-2222 is OWB.
相关器械（代码：OWB）
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官方来源
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