FDA 510(k)

MODEL 6208,6209,6210,6211,6212,6214 (PLI'S)

K-Number: K890045 · 1989-01-30

Decision Date1989-01-30

Product CodeDTB

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

MODEL 6208,6209,6210,6211,6212,6214 (PLI'S) is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1989-01-30 under 510(k) number K890045. The device is classified under product code DTB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 6208,6209,6210,6211,6212,6214 (PLI'S)?

MODEL 6208,6209,6210,6211,6212,6214 (PLI'S) is a medical device that received FDA 510(k) clearance on 1989-01-30. The listed applicant is Medtronic Vascular. The 510(k) number is K890045.

When did MODEL 6208,6209,6210,6211,6212,6214 (PLI'S) receive FDA 510(k) clearance?

MODEL 6208,6209,6210,6211,6212,6214 (PLI'S) received FDA 510(k) clearance on 1989-01-30, under 510(k) number K890045.

Who is the listed applicant for MODEL 6208,6209,6210,6211,6212,6214 (PLI'S)?

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

What is the FDA product code for MODEL 6208,6209,6210,6211,6212,6214 (PLI'S)?

The FDA product code for MODEL 6208,6209,6210,6211,6212,6214 (PLI'S) is DTB.

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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.