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FDA 510(k)

VIADUCT MINISCOPE AND ACCESSORIES

K-Number: K040949 · 2004-05-07

ApplicantAcueity, Inc.
Decision Date2004-05-07
Product CodeGCT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

VIADUCT MINISCOPE AND ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Acueity, Inc.. It received FDA 510(k) clearance on 2004-05-07 under 510(k) number K040949. The device is classified under product code GCT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIADUCT MINISCOPE AND ACCESSORIES?

VIADUCT MINISCOPE AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 2004-05-07. The listed applicant is Acueity, Inc.. The 510(k) number is K040949.

When did VIADUCT MINISCOPE AND ACCESSORIES receive FDA 510(k) clearance?

VIADUCT MINISCOPE AND ACCESSORIES received FDA 510(k) clearance on 2004-05-07, under 510(k) number K040949.

Who is the listed applicant for VIADUCT MINISCOPE AND ACCESSORIES?

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

What is the FDA product code for VIADUCT MINISCOPE AND ACCESSORIES?

The FDA product code for VIADUCT MINISCOPE AND ACCESSORIES is GCT.

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 Acueity, Inc. 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.

K032847EXCISOR BIOPTOME, MODEL 01-0004K032430ACUEITY MEDICAL LIGHT SOURCEK011189VIADUCT MICROENDOSCOPE AND ACCESSORIES

Related Devices (Code: GCT)

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.

K093125ALPHAXENON LIGHT 180 W AND 300 WGimmi GmbHK082925XENON-100 SCB LIGHT SOURCE, MODEL 20132620KARL STORZ Endoscopy-America, Inc.K070376CONMED LINVATEC 300W XENON LIGHT SOURCEConmed LinvatecK022490KSEA MEDI PACKKARL STORZ Endoscopy-America, Inc.K031994LINVATEC 300W XENON LIGHT SOURCELinvatec Corp.K023468ENDOSCOPIC LIGHT SOURCE XL180/L3World of Medicine Lemke GmbH

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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