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FDA 510(k)

CAPTIVA BLOOD CONTAINMENT DEVICE CN100, CAN19T71W

K-Number: K031922 · 2003-10-01

ApplicantMerit Medical Systems, Inc.
Decision Date2003-10-01
Product CodeDYB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CAPTIVA BLOOD CONTAINMENT DEVICE CN100, CAN19T71W is the device name listed in this FDA 510(k) record. The listed applicant is Merit Medical Systems, Inc.. It received FDA 510(k) clearance on 2003-10-01 under 510(k) number K031922. The device is classified under product code DYB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAPTIVA BLOOD CONTAINMENT DEVICE CN100, CAN19T71W?

CAPTIVA BLOOD CONTAINMENT DEVICE CN100, CAN19T71W is a medical device that received FDA 510(k) clearance on 2003-10-01. The listed applicant is Merit Medical Systems, Inc.. The 510(k) number is K031922.

When did CAPTIVA BLOOD CONTAINMENT DEVICE CN100, CAN19T71W receive FDA 510(k) clearance?

CAPTIVA BLOOD CONTAINMENT DEVICE CN100, CAN19T71W received FDA 510(k) clearance on 2003-10-01, under 510(k) number K031922.

Who is the listed applicant for CAPTIVA BLOOD CONTAINMENT DEVICE CN100, CAN19T71W?

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

What is the FDA product code for CAPTIVA BLOOD CONTAINMENT DEVICE CN100, CAN19T71W?

The FDA product code for CAPTIVA BLOOD CONTAINMENT DEVICE CN100, CAN19T71W is DYB.

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Related Devices (Code: DYB)

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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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