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FDA 510(k)

RADIUS SNARE

K-Number: K070502 · 2007-10-04

ApplicantRadius Medical Technologies, Inc.
Decision Date2007-10-04
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

RADIUS SNARE is the device name listed in this FDA 510(k) record. The listed applicant is Radius Medical Technologies, Inc.. It received FDA 510(k) clearance on 2007-10-04 under 510(k) number K070502. 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 RADIUS SNARE?

RADIUS SNARE is a medical device that received FDA 510(k) clearance on 2007-10-04. The listed applicant is Radius Medical Technologies, Inc.. The 510(k) number is K070502.

When did RADIUS SNARE receive FDA 510(k) clearance?

RADIUS SNARE received FDA 510(k) clearance on 2007-10-04, under 510(k) number K070502.

Who is the listed applicant for RADIUS SNARE?

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

What is the FDA product code for RADIUS SNARE?

The FDA product code for RADIUS SNARE is DQY.

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 Radius Medical Technologies, 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.

K071457MODIFICATION TO RADIUS SNAREK032899RADIUS COUGAR WIREK032129RADIUS 018 COUGAR WIREK022201RADIUS MICRO SNAREK021441RADIUS SNAREK011759RADIUS NEXT GENERATION GUIDEWIRE

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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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