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FDA 510(k)

DUAL-LUMEN CATHETER

K-Number: K024165 · 2003-01-10

ApplicantBistech, Inc.
Decision Date2003-01-10
Product CodeEOQ
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

DUAL-LUMEN CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Bistech, Inc.. It received FDA 510(k) clearance on 2003-01-10 under 510(k) number K024165. The device is classified under product code EOQ. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUAL-LUMEN CATHETER?

DUAL-LUMEN CATHETER is a medical device that received FDA 510(k) clearance on 2003-01-10. The listed applicant is Bistech, Inc.. The 510(k) number is K024165.

When did DUAL-LUMEN CATHETER receive FDA 510(k) clearance?

DUAL-LUMEN CATHETER received FDA 510(k) clearance on 2003-01-10, under 510(k) number K024165.

Who is the listed applicant for DUAL-LUMEN CATHETER?

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

What is the FDA product code for DUAL-LUMEN CATHETER?

The FDA product code for DUAL-LUMEN CATHETER is EOQ.

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Related Devices (Code: EOQ)

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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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