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FDA 510(k)

AMPLATZER TORQVUE DELIVERY SYSTEM

K-Number: K072313 · 2007-11-02

ApplicantAga Medical Corp.
Decision Date2007-11-02
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

AMPLATZER TORQVUE DELIVERY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Aga Medical Corp.. It received FDA 510(k) clearance on 2007-11-02 under 510(k) number K072313. 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 AMPLATZER TORQVUE DELIVERY SYSTEM?

AMPLATZER TORQVUE DELIVERY SYSTEM is a medical device that received FDA 510(k) clearance on 2007-11-02. The listed applicant is Aga Medical Corp.. The 510(k) number is K072313.

When did AMPLATZER TORQVUE DELIVERY SYSTEM receive FDA 510(k) clearance?

AMPLATZER TORQVUE DELIVERY SYSTEM received FDA 510(k) clearance on 2007-11-02, under 510(k) number K072313.

Who is the listed applicant for AMPLATZER TORQVUE DELIVERY SYSTEM?

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

What is the FDA product code for AMPLATZER TORQVUE DELIVERY SYSTEM?

The FDA product code for AMPLATZER TORQVUE DELIVERY SYSTEM is DQY.

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Other records listing Aga Medical 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.

K113658AMPLATZER VASCULAR PLUG 4K093476AMPLATZER TORQ VUE 2 DELIVERY SHEATH MODEL 9-TV2-05F120, MODEL 9-TV2-06F120, MODELTV-2-07F120K091793AMPLATZER TORQVUE 3 DELIVERY SHEATH, MODEL 9-TV3-08F104, 9-TV3-08F54K083214AMPLATZER TORQVUE 45DEGREEX45DEGREE DELIVERY SHEATH, MODELS 9-TV45X45-09F-100, 9-TV45X45-10F-100K080994AMPLATZER TORQVUE EXCHANGE SYSTEMK080757AMPLATZER TORQVUE LOW PROFILE DELIVERY SYSTEM

View all 14 devices →

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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