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FDA 510(k)

TEMPORARY SCREENING LEAD/ CATHETER KIT

K-Number: K934939 · 1995-05-24

ApplicantMedtronic Vascular
Decision Date1995-05-24
Product CodeMAJ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

TEMPORARY SCREENING LEAD/ CATHETER KIT is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1995-05-24 under 510(k) number K934939. The device is classified under product code MAJ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TEMPORARY SCREENING LEAD/ CATHETER KIT?

TEMPORARY SCREENING LEAD/ CATHETER KIT is a medical device that received FDA 510(k) clearance on 1995-05-24. The listed applicant is Medtronic Vascular. The 510(k) number is K934939.

When did TEMPORARY SCREENING LEAD/ CATHETER KIT receive FDA 510(k) clearance?

TEMPORARY SCREENING LEAD/ CATHETER KIT received FDA 510(k) clearance on 1995-05-24, under 510(k) number K934939.

Who is the listed applicant for TEMPORARY SCREENING LEAD/ CATHETER KIT?

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 TEMPORARY SCREENING LEAD/ CATHETER KIT?

The FDA product code for TEMPORARY SCREENING LEAD/ CATHETER KIT is MAJ.

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Other records listing Medtronic Vascular as applicant

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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: MAJ)

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.

K965251MEDTRONIC ALGOLINE INTRASPINAL CATHETER SYSTEMMedtronic VascularK945413MEDTRONIC MODEL 3864C & 3865C TEMPORARY SCREENING LEAD/CATHETER KITMedtronic VascularK930218SUBCUTANEOUS TUNNELING NEEDLE AND HANDLESConcord/PortexK911382IPI ALGO-LINE CATHETERPudenz-Schulte Medical Research Corp.K893766LIFECARE CONT. EPIDURAL CATH. FOR MORPHINE SULFATEAbbott Laboratories

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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