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FDA 510(k)

EASY RIDER MICRO CATHETER

K-Number: K974473 · 1998-06-17

Decision Date1998-06-17
Product CodeKRA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

EASY RIDER MICRO CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Micro Therapeutics, Inc.. It received FDA 510(k) clearance on 1998-06-17 under 510(k) number K974473. The device is classified under product code KRA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EASY RIDER MICRO CATHETER?

EASY RIDER MICRO CATHETER is a medical device that received FDA 510(k) clearance on 1998-06-17. The listed applicant is Micro Therapeutics, Inc.. The 510(k) number is K974473.

When did EASY RIDER MICRO CATHETER receive FDA 510(k) clearance?

EASY RIDER MICRO CATHETER received FDA 510(k) clearance on 1998-06-17, under 510(k) number K974473.

Who is the listed applicant for EASY RIDER MICRO CATHETER?

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

What is the FDA product code for EASY RIDER MICRO CATHETER?

The FDA product code for EASY RIDER MICRO CATHETER is KRA.

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.

Other records listing Micro Therapeutics, 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.

View all 51 devices →

Related Devices (Code: KRA)

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.

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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