FDA 510(k)

MEDTRONIC 6210 PERMANENT LEAD INTRODUC

K-Number: K842780 · 1984-08-03

Decision Date1984-08-03

Product CodeDYB

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

MEDTRONIC 6210 PERMANENT LEAD INTRODUC is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1984-08-03 under 510(k) number K842780. 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 MEDTRONIC 6210 PERMANENT LEAD INTRODUC?

MEDTRONIC 6210 PERMANENT LEAD INTRODUC is a medical device that received FDA 510(k) clearance on 1984-08-03. The listed applicant is Medtronic Vascular. The 510(k) number is K842780.

When did MEDTRONIC 6210 PERMANENT LEAD INTRODUC receive FDA 510(k) clearance?

MEDTRONIC 6210 PERMANENT LEAD INTRODUC received FDA 510(k) clearance on 1984-08-03, under 510(k) number K842780.

Who is the listed applicant for MEDTRONIC 6210 PERMANENT LEAD INTRODUC?

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 MEDTRONIC 6210 PERMANENT LEAD INTRODUC?

The FDA product code for MEDTRONIC 6210 PERMANENT LEAD INTRODUC 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.