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FDA 510(k)

MODIFIED CONCENTRIC RETRIEVER, MODEL 90039

K-Number: K051838 · 2005-09-01

ApplicantConcentric Medical, Inc.
Decision Date2005-09-01
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODIFIED CONCENTRIC RETRIEVER, MODEL 90039 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 2005-09-01 under 510(k) number K051838. 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 MODIFIED CONCENTRIC RETRIEVER, MODEL 90039?

MODIFIED CONCENTRIC RETRIEVER, MODEL 90039 is a medical device that received FDA 510(k) clearance on 2005-09-01. The listed applicant is Concentric Medical, Inc.. The 510(k) number is K051838.

When did MODIFIED CONCENTRIC RETRIEVER, MODEL 90039 receive FDA 510(k) clearance?

MODIFIED CONCENTRIC RETRIEVER, MODEL 90039 received FDA 510(k) clearance on 2005-09-01, under 510(k) number K051838.

Who is the listed applicant for MODIFIED CONCENTRIC RETRIEVER, MODEL 90039?

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 MODIFIED CONCENTRIC RETRIEVER, MODEL 90039?

The FDA product code for MODIFIED CONCENTRIC RETRIEVER, MODEL 90039 is DQY.

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Other records listing Concentric Medical, Inc. as applicant

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Related Devices (Code: DQY)

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.

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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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