FDA 510(k)

MODELS 6207/6208/6209/6210/6211/6212/6214 (PLI'S)

K-Number: K900515 · 1990-08-23

Decision Date1990-08-23

Product CodeDYB

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

MODELS 6207/6208/6209/6210/6211/6212/6214 (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 1990-08-23 under 510(k) number K900515. 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 MODELS 6207/6208/6209/6210/6211/6212/6214 (PLI'S)?

MODELS 6207/6208/6209/6210/6211/6212/6214 (PLI'S) is a medical device that received FDA 510(k) clearance on 1990-08-23. The listed applicant is Medtronic Vascular. The 510(k) number is K900515.

When did MODELS 6207/6208/6209/6210/6211/6212/6214 (PLI'S) receive FDA 510(k) clearance?

MODELS 6207/6208/6209/6210/6211/6212/6214 (PLI'S) received FDA 510(k) clearance on 1990-08-23, under 510(k) number K900515.

Who is the listed applicant for MODELS 6207/6208/6209/6210/6211/6212/6214 (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 MODELS 6207/6208/6209/6210/6211/6212/6214 (PLI'S)?

The FDA product code for MODELS 6207/6208/6209/6210/6211/6212/6214 (PLI'S) is DYB.

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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.