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FDA 510(k)

MODIFIED MERCY RETRIEVER, MODEL 90070

K-Number: K070521 · 2007-04-24

ApplicantConcentric Medical, Inc.
Decision Date2007-04-24
Product CodeNRY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODIFIED MERCY RETRIEVER, MODEL 90070 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 2007-04-24 under 510(k) number K070521. 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 MODIFIED MERCY RETRIEVER, MODEL 90070?

MODIFIED MERCY RETRIEVER, MODEL 90070 is a medical device that received FDA 510(k) clearance on 2007-04-24. The listed applicant is Concentric Medical, Inc.. The 510(k) number is K070521.

When did MODIFIED MERCY RETRIEVER, MODEL 90070 receive FDA 510(k) clearance?

MODIFIED MERCY RETRIEVER, MODEL 90070 received FDA 510(k) clearance on 2007-04-24, under 510(k) number K070521.

Who is the listed applicant for MODIFIED MERCY RETRIEVER, MODEL 90070?

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 MERCY RETRIEVER, MODEL 90070?

The FDA product code for MODIFIED MERCY RETRIEVER, MODEL 90070 is NRY.

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Related Devices (Code: NRY)

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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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