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FDA 510(k)

MODEL 2872 BIPOLAR LEAD ADAPTOR KIT

K-Number: K982220 · 1998-10-15

Decision Date1998-10-15
Product CodeDTD
Advisory CommitteeCV
DecisionSubstantially Equivalent - Subject to Tracking Reg.

Device Summary

MODEL 2872 BIPOLAR LEAD ADAPTOR KIT is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1998-10-15 under 510(k) number K982220. The device is classified under product code DTD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent - Subject to Tracking Reg..

Frequently Asked Questions

What is the MODEL 2872 BIPOLAR LEAD ADAPTOR KIT?

MODEL 2872 BIPOLAR LEAD ADAPTOR KIT is a medical device that received FDA 510(k) clearance on 1998-10-15. The listed applicant is Medtronic Vascular. The 510(k) number is K982220.

When did MODEL 2872 BIPOLAR LEAD ADAPTOR KIT receive FDA 510(k) clearance?

MODEL 2872 BIPOLAR LEAD ADAPTOR KIT received FDA 510(k) clearance on 1998-10-15, under 510(k) number K982220.

Who is the listed applicant for MODEL 2872 BIPOLAR LEAD ADAPTOR KIT?

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 2872 BIPOLAR LEAD ADAPTOR KIT?

The FDA product code for MODEL 2872 BIPOLAR LEAD ADAPTOR KIT is DTD.

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: DTD)

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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