FDA 510(k)

CFP-3131, CFP-2222

K 號：K201172 · 2020-05-29

決定日期2020-05-29

產品代碼OWB

諮詢委員會RA

決定相當於

器材摘要

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.

常見問題

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.

相關器械（代碼：OWB）

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。

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官方來源

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