FDA 510(k)

SEGUE INFUSION CATHETER

K-Number: K964154 · 1997-01-14

ApplicantInterventional Innovations Corp.

Decision Date1997-01-14

Product CodeKRA

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

SEGUE INFUSION CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Interventional Innovations Corp.. It received FDA 510(k) clearance on 1997-01-14 under 510(k) number K964154. The device is classified under product code KRA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SEGUE INFUSION CATHETER?

SEGUE INFUSION CATHETER is a medical device that received FDA 510(k) clearance on 1997-01-14. The listed applicant is Interventional Innovations Corp.. The 510(k) number is K964154.

When did SEGUE INFUSION CATHETER receive FDA 510(k) clearance?

SEGUE INFUSION CATHETER received FDA 510(k) clearance on 1997-01-14, under 510(k) number K964154.

Who is the listed applicant for SEGUE INFUSION CATHETER?

The FDA 510(k) record lists Interventional Innovations Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SEGUE INFUSION CATHETER?

The FDA product code for SEGUE INFUSION CATHETER is KRA.

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Other records listing Interventional Innovations Corp. as applicant

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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.