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FDA 510(k)

UNIVERSAL DELIVERY SYSTEM CATHETER

K-Number: K900657 · 1990-05-09

ApplicantMicrovena Corp.
Decision Date1990-05-09
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

UNIVERSAL DELIVERY SYSTEM CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Microvena Corp.. It received FDA 510(k) clearance on 1990-05-09 under 510(k) number K900657. 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 UNIVERSAL DELIVERY SYSTEM CATHETER?

UNIVERSAL DELIVERY SYSTEM CATHETER is a medical device that received FDA 510(k) clearance on 1990-05-09. The listed applicant is Microvena Corp.. The 510(k) number is K900657.

When did UNIVERSAL DELIVERY SYSTEM CATHETER receive FDA 510(k) clearance?

UNIVERSAL DELIVERY SYSTEM CATHETER received FDA 510(k) clearance on 1990-05-09, under 510(k) number K900657.

Who is the listed applicant for UNIVERSAL DELIVERY SYSTEM CATHETER?

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 UNIVERSAL DELIVERY SYSTEM CATHETER?

The FDA product code for UNIVERSAL DELIVERY SYSTEM CATHETER 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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