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FDA 510(k)

MERCI RETRIEVER, MODELS 90065, 90066

K-Number: K033736 · 2004-08-11

ApplicantConcentric Medical, Inc.
Decision Date2004-08-11
Product CodeNRY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MERCI RETRIEVER, MODELS 90065, 90066 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 2004-08-11 under 510(k) number K033736. The device is classified under product code NRY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MERCI RETRIEVER, MODELS 90065, 90066?

MERCI RETRIEVER, MODELS 90065, 90066 is a medical device that received FDA 510(k) clearance on 2004-08-11. The listed applicant is Concentric Medical, Inc.. The 510(k) number is K033736.

When did MERCI RETRIEVER, MODELS 90065, 90066 receive FDA 510(k) clearance?

MERCI RETRIEVER, MODELS 90065, 90066 received FDA 510(k) clearance on 2004-08-11, under 510(k) number K033736.

Who is the listed applicant for MERCI RETRIEVER, MODELS 90065, 90066?

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 MERCI RETRIEVER, MODELS 90065, 90066?

The FDA product code for MERCI RETRIEVER, MODELS 90065, 90066 is NRY.

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Other records listing Concentric Medical, Inc. as applicant

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Related Devices (Code: NRY)

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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