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FDA 510(k)

MEDTRONIC PERMANENT LEAD INTRODUCER

K-Number: K874167 · 1987-12-07

ApplicantMedtronic Vascular
Decision Date1987-12-07
Product CodeDTB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEDTRONIC PERMANENT LEAD INTRODUCER is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1987-12-07 under 510(k) number K874167. 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 PERMANENT LEAD INTRODUCER?

MEDTRONIC PERMANENT LEAD INTRODUCER is a medical device that received FDA 510(k) clearance on 1987-12-07. The listed applicant is Medtronic Vascular. The 510(k) number is K874167.

When did MEDTRONIC PERMANENT LEAD INTRODUCER receive FDA 510(k) clearance?

MEDTRONIC PERMANENT LEAD INTRODUCER received FDA 510(k) clearance on 1987-12-07, under 510(k) number K874167.

Who is the listed applicant for MEDTRONIC PERMANENT LEAD INTRODUCER?

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 PERMANENT LEAD INTRODUCER?

The FDA product code for MEDTRONIC PERMANENT LEAD INTRODUCER 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.

K232570Steerant™ Super Stiff GuidewireK2321906F Sherpa NX Balanced Guide Catheter, 7F Sherpa NX Balanced Guide CatheterK2301565F Launcher Guide Catheter, 6F Launcher Guide Catheter, 7F Launcher Guide Catheter, 8F Launcher Guide CatheterK220773Everest 20 Inflation Device and 3-way Stopcock (AC2200);Everest 30 Inflation Device and 3-way Stopcock (AC3200);Everest 20 Survival Kit containing:1. Everest 20 Device with 3-way Stopcock, 2. Piton Y-Adaptor ,3. Metal Guidewire Insertion Needle, 4. Torque Handle (AC2205P); Everest 30 Survival Kit containing:1. Everest 30 Device with 3-way Stopcock, 2. Piton Y-Adaptor,3. Metal Guidewire Insertion Needle, 4. Torque Handle (AC3205P)K192296Medtronic 6F Taiga Guiding CatheterK173515Admiral Xtreme

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.

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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