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FDA 510(k)

TRANSVENOUS, PERMANENT TINED TARGET TIP PACING LEADS

K-Number: K951858 · 1995-10-12

Decision Date1995-10-12
Product CodeDTB
Advisory CommitteeCV
DecisionSubstantially Equivalent - Subject to Tracking Reg.

Device Summary

TRANSVENOUS, PERMANENT TINED TARGET TIP PACING LEADS is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1995-10-12 under 510(k) number K951858. The device is classified under product code DTB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent - Subject to Tracking Reg..

Frequently Asked Questions

What is the TRANSVENOUS, PERMANENT TINED TARGET TIP PACING LEADS?

TRANSVENOUS, PERMANENT TINED TARGET TIP PACING LEADS is a medical device that received FDA 510(k) clearance on 1995-10-12. The listed applicant is Medtronic Vascular. The 510(k) number is K951858.

When did TRANSVENOUS, PERMANENT TINED TARGET TIP PACING LEADS receive FDA 510(k) clearance?

TRANSVENOUS, PERMANENT TINED TARGET TIP PACING LEADS received FDA 510(k) clearance on 1995-10-12, under 510(k) number K951858.

Who is the listed applicant for TRANSVENOUS, PERMANENT TINED TARGET TIP PACING LEADS?

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 TRANSVENOUS, PERMANENT TINED TARGET TIP PACING LEADS?

The FDA product code for TRANSVENOUS, PERMANENT TINED TARGET TIP PACING LEADS is DTB.

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: DTB)

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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