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FDA 510(k)

INFUSIONCATH

K-Number: K041517 · 2004-08-05

ApplicantId, LLC
Decision Date2004-08-05
Product CodeQEY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

INFUSIONCATH is the device name listed in this FDA 510(k) record. The listed applicant is Id, LLC. It received FDA 510(k) clearance on 2004-08-05 under 510(k) number K041517. The device is classified under product code QEY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INFUSIONCATH?

INFUSIONCATH is a medical device that received FDA 510(k) clearance on 2004-08-05. The listed applicant is Id, LLC. The 510(k) number is K041517.

When did INFUSIONCATH receive FDA 510(k) clearance?

INFUSIONCATH received FDA 510(k) clearance on 2004-08-05, under 510(k) number K041517.

Who is the listed applicant for INFUSIONCATH?

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

What is the FDA product code for INFUSIONCATH?

The FDA product code for INFUSIONCATH is QEY.

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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.

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