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FDA 510(k)

PACING LEAD MODEL 6991A

K-Number: K772104 · 1977-11-28

Decision Date1977-11-28
Product CodeDTB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PACING LEAD MODEL 6991A is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1977-11-28 under 510(k) number K772104. The device is classified under product code DTB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PACING LEAD MODEL 6991A?

PACING LEAD MODEL 6991A is a medical device that received FDA 510(k) clearance on 1977-11-28. The listed applicant is Medtronic Vascular. The 510(k) number is K772104.

When did PACING LEAD MODEL 6991A receive FDA 510(k) clearance?

PACING LEAD MODEL 6991A received FDA 510(k) clearance on 1977-11-28, under 510(k) number K772104.

Who is the listed applicant for PACING LEAD MODEL 6991A?

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 PACING LEAD MODEL 6991A?

The FDA product code for PACING LEAD MODEL 6991A 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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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