FDA 510(k)

CONCENTRIC MICRO CATHETER, MODELS 90001 TO 90008

K-Number: K003086 · 2001-05-16

Decision Date2001-05-16

Product CodeDQO

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

CONCENTRIC MICRO CATHETER, MODELS 90001 TO 90008 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 2001-05-16 under 510(k) number K003086. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONCENTRIC MICRO CATHETER, MODELS 90001 TO 90008?

CONCENTRIC MICRO CATHETER, MODELS 90001 TO 90008 is a medical device that received FDA 510(k) clearance on 2001-05-16. The listed applicant is Concentric Medical, Inc.. The 510(k) number is K003086.

When did CONCENTRIC MICRO CATHETER, MODELS 90001 TO 90008 receive FDA 510(k) clearance?

CONCENTRIC MICRO CATHETER, MODELS 90001 TO 90008 received FDA 510(k) clearance on 2001-05-16, under 510(k) number K003086.

Who is the listed applicant for CONCENTRIC MICRO CATHETER, MODELS 90001 TO 90008?

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 MICRO CATHETER, MODELS 90001 TO 90008?

The FDA product code for CONCENTRIC MICRO CATHETER, MODELS 90001 TO 90008 is DQO.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.