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FDA 510(k)

CONCENTRIC RETRIEVER, MODEL 90030

K-Number: K003410 · 2001-05-22

ApplicantConcentric Medical, Inc.
Decision Date2001-05-22
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CONCENTRIC RETRIEVER, MODEL 90030 is the device name listed in this FDA 510(k) record. The listed applicant is Concentric Medical, Inc.. It received FDA 510(k) clearance on 2001-05-22 under 510(k) number K003410. 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 CONCENTRIC RETRIEVER, MODEL 90030?

CONCENTRIC RETRIEVER, MODEL 90030 is a medical device that received FDA 510(k) clearance on 2001-05-22. The listed applicant is Concentric Medical, Inc.. The 510(k) number is K003410.

When did CONCENTRIC RETRIEVER, MODEL 90030 receive FDA 510(k) clearance?

CONCENTRIC RETRIEVER, MODEL 90030 received FDA 510(k) clearance on 2001-05-22, under 510(k) number K003410.

Who is the listed applicant for CONCENTRIC RETRIEVER, MODEL 90030?

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

What is the FDA product code for CONCENTRIC RETRIEVER, MODEL 90030?

The FDA product code for CONCENTRIC RETRIEVER, MODEL 90030 is DQY.

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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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