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FDA 510(k)

MERILAS 532A

K-Number: K072823 · 2007-12-14

ApplicantMeridian AG
Decision Date2007-12-14
Product CodeHQF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MERILAS 532A is the device name listed in this FDA 510(k) record. The listed applicant is Meridian AG. It received FDA 510(k) clearance on 2007-12-14 under 510(k) number K072823. 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 MERILAS 532A?

MERILAS 532A is a medical device that received FDA 510(k) clearance on 2007-12-14. The listed applicant is Meridian AG. The 510(k) number is K072823.

When did MERILAS 532A receive FDA 510(k) clearance?

MERILAS 532A received FDA 510(k) clearance on 2007-12-14, under 510(k) number K072823.

Who is the listed applicant for MERILAS 532A?

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 MERILAS 532A?

The FDA product code for MERILAS 532A is HQF.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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.

K232417MR Q; MR Q SUPINE; MR Q SLTK231011Merilas 532 shortpulse, Merilas 577 shortpulse, Merilas 810 shortpulseK160677MICRORUPTOR 6K113390LASER INDIRECT OPHTHALMOSCOPE 500(LIO-500)K023045MICRORUPTER V

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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