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FDA 510(k)

MR Q; MR Q SUPINE; MR Q SLT

K-Number: K232417 · 2024-01-25

ApplicantMeridian AG
Decision Date2024-01-25
Product CodeHQF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MR Q; MR Q SUPINE; MR Q SLT is the device name listed in this FDA 510(k) record. The listed applicant is Meridian AG. It received FDA 510(k) clearance on 2024-01-25 under 510(k) 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. The listed applicant is Meridian AG. The 510(k) number is K232417.

When did MR Q; MR Q SUPINE; MR Q SLT receive FDA 510(k) clearance?

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

Who is the listed applicant for MR Q; MR Q SUPINE; MR Q SLT?

The FDA 510(k) record lists Meridian AG as the applicant. This does not by itself establish the device manufacturer.

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 records listing Meridian AG as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K231011Merilas 532 shortpulse, Merilas 577 shortpulse, Merilas 810 shortpulseK160677MICRORUPTOR 6

Related Devices (Code: HQF)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K252979Voyager DSLT (430840610)Belkin Vision, Ltd.K251507INTEGRE LIOQuantel MedicalK251772Navilas Laser System 577sl (156691)Od-Os GmbHK243014EyeQ nanoECPEyeq, Inc.K240615Leos Laser and Endoscopy SystemBeaver-Visitec International, Inc.K242397LYNX PhotocoagulatorNorlase Aps

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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