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FDA 510(k)

RADIUS MICRO SNARE

K-Number: K022201 · 2003-02-03

ApplicantRadius Medical Technologies, Inc.
Decision Date2003-02-03
Product CodeMMX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

RADIUS MICRO 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 2003-02-03 under 510(k) number K022201. The device is classified under product code MMX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RADIUS MICRO SNARE?

RADIUS MICRO SNARE is a medical device that received FDA 510(k) clearance on 2003-02-03. The listed applicant is Radius Medical Technologies, Inc.. The 510(k) number is K022201.

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

RADIUS MICRO SNARE received FDA 510(k) clearance on 2003-02-03, under 510(k) number K022201.

Who is the listed applicant for RADIUS MICRO 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 MICRO SNARE?

The FDA product code for RADIUS MICRO SNARE is MMX.

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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.

K070502RADIUS SNAREK071457MODIFICATION TO RADIUS SNAREK032899RADIUS COUGAR WIREK032129RADIUS 018 COUGAR WIREK021441RADIUS SNAREK011759RADIUS NEXT GENERATION GUIDEWIRE

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Related Devices (Code: MMX)

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.

K242776LimFlow V-CeiverLimFlow, Inc.K241259Amplatz Goose Neck Snare KitMedtronic, Inc.K232443Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval KitArgon Medical Devices, Inc.K222254Gunther Tulip Vena Cava Filter Retrieval SetCook IncorporatedK222083LimFlow V-CeiverLimFlow, Inc.K212988ONO Retrieval DeviceOnocor Vascular, LLC

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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