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FDA 510(k)

MODEL 6494 UNIPOLAR TEMPORARY MYOCARDIAL PACING WIRE

K-Number: K012459 · 2001-08-14

Decision Date2001-08-14
Product CodeLDF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODEL 6494 UNIPOLAR TEMPORARY MYOCARDIAL PACING WIRE is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 2001-08-14 under 510(k) number K012459. The device is classified under product code LDF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 6494 UNIPOLAR TEMPORARY MYOCARDIAL PACING WIRE?

MODEL 6494 UNIPOLAR TEMPORARY MYOCARDIAL PACING WIRE is a medical device that received FDA 510(k) clearance on 2001-08-14. The listed applicant is Medtronic Vascular. The 510(k) number is K012459.

When did MODEL 6494 UNIPOLAR TEMPORARY MYOCARDIAL PACING WIRE receive FDA 510(k) clearance?

MODEL 6494 UNIPOLAR TEMPORARY MYOCARDIAL PACING WIRE received FDA 510(k) clearance on 2001-08-14, under 510(k) number K012459.

Who is the listed applicant for MODEL 6494 UNIPOLAR TEMPORARY MYOCARDIAL PACING WIRE?

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 6494 UNIPOLAR TEMPORARY MYOCARDIAL PACING WIRE?

The FDA product code for MODEL 6494 UNIPOLAR TEMPORARY MYOCARDIAL PACING WIRE is LDF.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Medtronic Vascular as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 474 devices →

Related Devices (Code: LDF)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.

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