FDA 510(k)

MEDTRONIC STYLET KIT, MODELS 6282, 6293, AND 6254

K-Number: K010906 · 2001-04-05

Decision Date2001-04-05

Product CodeDRB

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

MEDTRONIC STYLET KIT, MODELS 6282, 6293, AND 6254 is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 2001-04-05 under 510(k) number K010906. The device is classified under product code DRB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDTRONIC STYLET KIT, MODELS 6282, 6293, AND 6254?

MEDTRONIC STYLET KIT, MODELS 6282, 6293, AND 6254 is a medical device that received FDA 510(k) clearance on 2001-04-05. The listed applicant is Medtronic Vascular. The 510(k) number is K010906.

When did MEDTRONIC STYLET KIT, MODELS 6282, 6293, AND 6254 receive FDA 510(k) clearance?

MEDTRONIC STYLET KIT, MODELS 6282, 6293, AND 6254 received FDA 510(k) clearance on 2001-04-05, under 510(k) number K010906.

Who is the listed applicant for MEDTRONIC STYLET KIT, MODELS 6282, 6293, AND 6254?

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 STYLET KIT, MODELS 6282, 6293, AND 6254?

The FDA product code for MEDTRONIC STYLET KIT, MODELS 6282, 6293, AND 6254 is DRB.

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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.