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FDA 510(k)

HAD1717MC

K-Number: K200018 · 2020-01-31

ApplicantH&Abyz
Decision Date2020-01-31
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

HAD1717MC is a medical device manufactured by H&Abyz. It received FDA 510(k) clearance on 2020-01-31 under approval number K200018. The device is classified under product code MQB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HAD1717MC?

HAD1717MC is a medical device that received FDA 510(k) clearance on 2020-01-31. It is manufactured by H&Abyz. The 510(k) number is K200018.

When was HAD1717MC approved by the FDA?

HAD1717MC received FDA 510(k) clearance on 2020-01-31, under approval number K200018.

What company makes HAD1717MC?

HAD1717MC is manufactured by H&Abyz.

What is the FDA product code for HAD1717MC?

The FDA product code for HAD1717MC is MQB.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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