RFA-1717DIG, RFA-1717DIC
K号: K212051 · 2021-08-25
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器械摘要
RFA-1717DIG, RFA-1717DIC is the device name listed in this FDA 510(k) record. The listed applicant is Astel, Inc.. It received FDA 510(k) clearance on 2021-08-25 under 510(k) number K212051. 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 RFA-1717DIG, RFA-1717DIC?
RFA-1717DIG, RFA-1717DIC is a medical device that received FDA 510(k) clearance on 2021-08-25. The listed applicant is Astel, Inc.. The 510(k) number is K212051.
When did RFA-1717DIG, RFA-1717DIC receive FDA 510(k) clearance?
RFA-1717DIG, RFA-1717DIC received FDA 510(k) clearance on 2021-08-25, under 510(k) number K212051.
Who is the listed applicant for RFA-1717DIG, RFA-1717DIC?
The FDA 510(k) record lists Astel, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RFA-1717DIG, RFA-1717DIC?
The FDA product code for RFA-1717DIG, RFA-1717DIC is MQB.
相关器械（代码：MQB）
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