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FDA 510(k)

MX30N(MX30TQS)

K-Number: K160346 · 2016-04-14

Decision Date2016-04-14
Product CodePGY
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MX30N(MX30TQS) is a medical device manufactured by Wide Corporation. It received FDA 510(k) clearance on 2016-04-14 under approval number K160346. The device is classified under product code PGY. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MX30N(MX30TQS)?

MX30N(MX30TQS) is a medical device that received FDA 510(k) clearance on 2016-04-14. It is manufactured by Wide Corporation. The 510(k) number is K160346.

When was MX30N(MX30TQS) approved by the FDA?

MX30N(MX30TQS) received FDA 510(k) clearance on 2016-04-14, under approval number K160346.

What company makes MX30N(MX30TQS)?

MX30N(MX30TQS) is manufactured by Wide Corporation.

What is the FDA product code for MX30N(MX30TQS)?

The FDA product code for MX30N(MX30TQS) is PGY.

Other Devices by Wide Corporation

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Related Devices (Code: PGY)

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.