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FDA 510(k)

MERIDAN FILTER SYSTEM- JUNGULAR/SUBECLAVIAN DELIVERY KIT

K-Number: K102511 · 2011-08-24

ApplicantC.R. Bard, Inc.
Decision Date2011-08-24
Product CodeDTK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MERIDAN FILTER SYSTEM- JUNGULAR/SUBECLAVIAN DELIVERY KIT is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 2011-08-24 under 510(k) number K102511. The device is classified under product code DTK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MERIDAN FILTER SYSTEM- JUNGULAR/SUBECLAVIAN DELIVERY KIT?

MERIDAN FILTER SYSTEM- JUNGULAR/SUBECLAVIAN DELIVERY KIT is a medical device that received FDA 510(k) clearance on 2011-08-24. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K102511.

When did MERIDAN FILTER SYSTEM- JUNGULAR/SUBECLAVIAN DELIVERY KIT receive FDA 510(k) clearance?

MERIDAN FILTER SYSTEM- JUNGULAR/SUBECLAVIAN DELIVERY KIT received FDA 510(k) clearance on 2011-08-24, under 510(k) number K102511.

Who is the listed applicant for MERIDAN FILTER SYSTEM- JUNGULAR/SUBECLAVIAN DELIVERY KIT?

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

What is the FDA product code for MERIDAN FILTER SYSTEM- JUNGULAR/SUBECLAVIAN DELIVERY KIT?

The FDA product code for MERIDAN FILTER SYSTEM- JUNGULAR/SUBECLAVIAN DELIVERY KIT is DTK.

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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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