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FDA 510(k)

EN-SNARE ENDOVASCULAR SNARE AND CATHETER

K-Number: K021606 · 2002-05-31

ApplicantMedical Device Technologies, Inc.
Decision Date2002-05-31
Product CodeMMX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

EN-SNARE ENDOVASCULAR SNARE AND CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Medical Device Technologies, Inc.. It received FDA 510(k) clearance on 2002-05-31 under 510(k) number K021606. 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 EN-SNARE ENDOVASCULAR SNARE AND CATHETER?

EN-SNARE ENDOVASCULAR SNARE AND CATHETER is a medical device that received FDA 510(k) clearance on 2002-05-31. The listed applicant is Medical Device Technologies, Inc.. The 510(k) number is K021606.

When did EN-SNARE ENDOVASCULAR SNARE AND CATHETER receive FDA 510(k) clearance?

EN-SNARE ENDOVASCULAR SNARE AND CATHETER received FDA 510(k) clearance on 2002-05-31, under 510(k) number K021606.

Who is the listed applicant for EN-SNARE ENDOVASCULAR SNARE AND CATHETER?

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

What is the FDA product code for EN-SNARE ENDOVASCULAR SNARE AND CATHETER?

The FDA product code for EN-SNARE ENDOVASCULAR SNARE AND CATHETER is MMX.

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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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