FDA 510(k)

MODELS 6917T, 6917AT & 4951M EPICARDIAL PACE LEADS

K-Number: K921124 · 1992-05-22

Decision Date1992-05-22

Product CodeDTB

Advisory CommitteeCV

DecisionUnknown

Device Summary

MODELS 6917T, 6917AT & 4951M EPICARDIAL PACE 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 1992-05-22 under 510(k) number K921124. The device is classified under product code DTB. It was reviewed by the CV advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the MODELS 6917T, 6917AT & 4951M EPICARDIAL PACE LEADS?

MODELS 6917T, 6917AT & 4951M EPICARDIAL PACE LEADS is a medical device that received FDA 510(k) clearance on 1992-05-22. The listed applicant is Medtronic Vascular. The 510(k) number is K921124.

When did MODELS 6917T, 6917AT & 4951M EPICARDIAL PACE LEADS receive FDA 510(k) clearance?

MODELS 6917T, 6917AT & 4951M EPICARDIAL PACE LEADS received FDA 510(k) clearance on 1992-05-22, under 510(k) number K921124.

Who is the listed applicant for MODELS 6917T, 6917AT & 4951M EPICARDIAL PACE 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 MODELS 6917T, 6917AT & 4951M EPICARDIAL PACE LEADS?

The FDA product code for MODELS 6917T, 6917AT & 4951M EPICARDIAL PACE LEADS is DTB.

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Related Devices (Code: DTB)

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 Vascular K031210MODEL 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.