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FDA 510(k)

MEDIPORT II MODEL MP-DL VASCULAR ACCESS PORT

K-Number: K870817 · 1987-07-30

ApplicantC.R. Bard, Inc.
Decision Date1987-07-30
Product CodeLJT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MEDIPORT II MODEL MP-DL VASCULAR ACCESS PORT 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 1987-07-30 under 510(k) number K870817. The device is classified under product code LJT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDIPORT II MODEL MP-DL VASCULAR ACCESS PORT?

MEDIPORT II MODEL MP-DL VASCULAR ACCESS PORT is a medical device that received FDA 510(k) clearance on 1987-07-30. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K870817.

When did MEDIPORT II MODEL MP-DL VASCULAR ACCESS PORT receive FDA 510(k) clearance?

MEDIPORT II MODEL MP-DL VASCULAR ACCESS PORT received FDA 510(k) clearance on 1987-07-30, under 510(k) number K870817.

Who is the listed applicant for MEDIPORT II MODEL MP-DL VASCULAR ACCESS PORT?

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 MEDIPORT II MODEL MP-DL VASCULAR ACCESS PORT?

The FDA product code for MEDIPORT II MODEL MP-DL VASCULAR ACCESS PORT is LJT.

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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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