FDA 510(k)

MR Q; MR Q SUPINE; MR Q SLT

K-Number: K232417 · 2024-01-25

Decision Date2024-01-25

Product CodeHQF

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

MR Q; MR Q SUPINE; MR Q SLT is a medical device manufactured by Meridian AG. It received FDA 510(k) clearance on 2024-01-25 under approval number K232417. The device is classified under product code HQF. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MR Q; MR Q SUPINE; MR Q SLT?

MR Q; MR Q SUPINE; MR Q SLT is a medical device that received FDA 510(k) clearance on 2024-01-25. It is manufactured by Meridian AG. The 510(k) number is K232417.

When was MR Q; MR Q SUPINE; MR Q SLT approved by the FDA?

MR Q; MR Q SUPINE; MR Q SLT received FDA 510(k) clearance on 2024-01-25, under approval number K232417.

What company makes MR Q; MR Q SUPINE; MR Q SLT?

MR Q; MR Q SUPINE; MR Q SLT is manufactured by Meridian AG.

What is the FDA product code for MR Q; MR Q SUPINE; MR Q SLT?

The FDA product code for MR Q; MR Q SUPINE; MR Q SLT is HQF.

Other Devices by Meridian AG

K160677MICRORUPTOR 6 K231011Merilas 532 shortpulse, Merilas 577 shortpulse, Merilas 810 shortpulse

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Official Source

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