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FDA 510(k)

THROMBOLYTIC BRUSH CATHETER

K-Number: K963925 · 1997-08-08

ApplicantMicro Therapeutics, Inc.
Decision Date1997-08-08
Product CodeMCW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

THROMBOLYTIC BRUSH 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 1997-08-08 under 510(k) number K963925. The device is classified under product code MCW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THROMBOLYTIC BRUSH CATHETER?

THROMBOLYTIC BRUSH CATHETER is a medical device that received FDA 510(k) clearance on 1997-08-08. The listed applicant is Micro Therapeutics, Inc.. The 510(k) number is K963925.

When did THROMBOLYTIC BRUSH CATHETER receive FDA 510(k) clearance?

THROMBOLYTIC BRUSH CATHETER received FDA 510(k) clearance on 1997-08-08, under 510(k) number K963925.

Who is the listed applicant for THROMBOLYTIC BRUSH 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 THROMBOLYTIC BRUSH CATHETER?

The FDA product code for THROMBOLYTIC BRUSH CATHETER is MCW.

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Other records listing Micro Therapeutics, Inc. as applicant

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Related Devices (Code: MCW)

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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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