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FDA 510(k)

LEAD, PACING, ATRIAL, ENDOCARDIAL, TINED

K-Number: K780621 · 1978-07-26

ApplicantMedtronic Vascular
Decision Date1978-07-26
Product CodeDTB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LEAD, PACING, ATRIAL, ENDOCARDIAL, TINED is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1978-07-26 under 510(k) number K780621. 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 LEAD, PACING, ATRIAL, ENDOCARDIAL, TINED?

LEAD, PACING, ATRIAL, ENDOCARDIAL, TINED is a medical device that received FDA 510(k) clearance on 1978-07-26. The listed applicant is Medtronic Vascular. The 510(k) number is K780621.

When did LEAD, PACING, ATRIAL, ENDOCARDIAL, TINED receive FDA 510(k) clearance?

LEAD, PACING, ATRIAL, ENDOCARDIAL, TINED received FDA 510(k) clearance on 1978-07-26, under 510(k) number K780621.

Who is the listed applicant for LEAD, PACING, ATRIAL, ENDOCARDIAL, TINED?

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 LEAD, PACING, ATRIAL, ENDOCARDIAL, TINED?

The FDA product code for LEAD, PACING, ATRIAL, ENDOCARDIAL, TINED is DTB.

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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.

K061212BIOTRONIK ENDOCARDIAL PACING LEADSBiotronik, Inc.K041809PERMANENT PACING LEAD, MODEL PY2Oscor, Inc.K040569PERMANENT PACING LEAD, MODEL REFINO, MODEL: REFINO-R, RU, RJUOscor, Inc.K031274MODEL 5071 MYOCARDIAL PACING LEADMedtronic VascularK031210MODEL 4951M MYOCARDIAL UNIPOLAR LEADMetronic, Inc.K023205ELOX P 45-BP; ELOX P 53-BP; ELOX P 60-BPBiotronik, Inc.

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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