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FDA 510(k)

MEDTRONIC MODEL 5013

K-Number: K863536 · 1987-01-06

ApplicantMedtronic Vascular
Decision Date1987-01-06
Product CodeDTB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEDTRONIC MODEL 5013 is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1987-01-06 under 510(k) number K863536. 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 MEDTRONIC MODEL 5013?

MEDTRONIC MODEL 5013 is a medical device that received FDA 510(k) clearance on 1987-01-06. The listed applicant is Medtronic Vascular. The 510(k) number is K863536.

When did MEDTRONIC MODEL 5013 receive FDA 510(k) clearance?

MEDTRONIC MODEL 5013 received FDA 510(k) clearance on 1987-01-06, under 510(k) number K863536.

Who is the listed applicant for MEDTRONIC MODEL 5013?

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 MEDTRONIC MODEL 5013?

The FDA product code for MEDTRONIC MODEL 5013 is DTB.

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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.

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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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