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FDA 510(k)

VIADUCT MICROENDOSCOPE AND ACCESSORIES

K-Number: K011189 · 2001-07-16

ApplicantAcueity, Inc.
Decision Date2001-07-16
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

VIADUCT MICROENDOSCOPE 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 2001-07-16 under 510(k) number K011189. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIADUCT MICROENDOSCOPE AND ACCESSORIES?

VIADUCT MICROENDOSCOPE AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 2001-07-16. The listed applicant is Acueity, Inc.. The 510(k) number is K011189.

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

VIADUCT MICROENDOSCOPE AND ACCESSORIES received FDA 510(k) clearance on 2001-07-16, under 510(k) number K011189.

Who is the listed applicant for VIADUCT MICROENDOSCOPE 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 MICROENDOSCOPE AND ACCESSORIES?

The FDA product code for VIADUCT MICROENDOSCOPE AND ACCESSORIES is GCJ.

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.

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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.

K040949VIADUCT MINISCOPE AND ACCESSORIESK032847EXCISOR BIOPTOME, MODEL 01-0004K032430ACUEITY MEDICAL LIGHT SOURCE

Related Devices (Code: GCJ)

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.

K262397CuratOR EX2742Eizo CorporationK260884UNIDRIVE Select SystemKarl Storz SE & CO. KGK260972OEV-271MUH LCD Monitor;OEV-321MUH LCD Monitor;OEV-431MUH LCD MonitorSony CorporationK261139VereSee (VER150, VER200, VER151, VER201, VER200C, and VER-100-103)Freyja Healthcare, LLCK253541EZ-Close™ (EZ Close Port Site Closing Device, EZ Close MAX Port Site Closing Device, EZ Close II Port Site Closing Device)Medical ImpactK261614LED LCD Monitor (OEV-271H)Lg Electronics.Inc

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.

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