HAD1717MC
K号: K200018 · 2020-01-31
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器械摘要
HAD1717MC is the device name listed in this FDA 510(k) record. The listed applicant is H&Abyz. It received FDA 510(k) clearance on 2020-01-31 under 510(k) number K200018. 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 HAD1717MC?
HAD1717MC is a medical device that received FDA 510(k) clearance on 2020-01-31. The listed applicant is H&Abyz. The 510(k) number is K200018.
When did HAD1717MC receive FDA 510(k) clearance?
HAD1717MC received FDA 510(k) clearance on 2020-01-31, under 510(k) number K200018.
Who is the listed applicant for HAD1717MC?
The FDA 510(k) record lists H&Abyz as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HAD1717MC?
The FDA product code for HAD1717MC is MQB.
相关器械（代码：MQB）
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官方来源
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