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FDA 510(k)

MICROSNARE

K-Number: K925439 · 1993-09-24

ApplicantMicrovena Corp.
Decision Date1993-09-24
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MICROSNARE is the device name listed in this FDA 510(k) record. The listed applicant is Microvena Corp.. It received FDA 510(k) clearance on 1993-09-24 under 510(k) number K925439. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROSNARE?

MICROSNARE is a medical device that received FDA 510(k) clearance on 1993-09-24. The listed applicant is Microvena Corp.. The 510(k) number is K925439.

When did MICROSNARE receive FDA 510(k) clearance?

MICROSNARE received FDA 510(k) clearance on 1993-09-24, under 510(k) number K925439.

Who is the listed applicant for MICROSNARE?

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

What is the FDA product code for MICROSNARE?

The FDA product code for MICROSNARE is DQY.

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Other records listing Microvena Corp. 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.

K991898ULTRA-SELECT GUIDEWIRE, HYTEK GUIDEWIREK991194MODIFICATION TO ULTRA-SELECT GUIDEWIREK982657AMPLATZ THROMBECTOMY DEVICE MODELS ATD 601, ATD 602, ATD 801, ATD 802, FOOT PEDAL ASSEMBLY MODEL AK 100K970668THE AMPLANTZ GOOSE NECK MICROSNAREK972511AMPLATZ GOOSE NECK SNARE KIT/ CATHETERK971984AMPLATZ THROMBECTOMY DEVICE(ATD 603,602,801,802)/FOOT PEDAL ASSEMBLY(AK 200)

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Related Devices (Code: DQY)

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.

K262817CrossFAST Integrated Microcatheter Advanced Delivery SystemVantis Vascular, Inc.K260559NHanceITIMDS Operation B.V.K262392APRO 35 Swift CatheterAlembic, LLCK262240SSPC NXT Delivery CatheterCenterPoint Systems, LLCK261766CPS Locator 3D Plus Delivery CatheterCenterPoint Systems, LLCK261825Amplatzer TorqVue LP Delivery System; Amplatzer TorqVue LP CatheterAbbott

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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