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FDA 510(k)

J-LLOYD ARTERIAL EMBOLECTOMY CATHETER

K-Number: K920871 · 1993-02-26

ApplicantJ-Lloyd Medical, Inc.
Decision Date1993-02-26
Product CodeDXE
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

J-LLOYD ARTERIAL EMBOLECTOMY CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is J-Lloyd Medical, Inc.. It received FDA 510(k) clearance on 1993-02-26 under 510(k) number K920871. The device is classified under product code DXE. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the J-LLOYD ARTERIAL EMBOLECTOMY CATHETER?

J-LLOYD ARTERIAL EMBOLECTOMY CATHETER is a medical device that received FDA 510(k) clearance on 1993-02-26. The listed applicant is J-Lloyd Medical, Inc.. The 510(k) number is K920871.

When did J-LLOYD ARTERIAL EMBOLECTOMY CATHETER receive FDA 510(k) clearance?

J-LLOYD ARTERIAL EMBOLECTOMY CATHETER received FDA 510(k) clearance on 1993-02-26, under 510(k) number K920871.

Who is the listed applicant for J-LLOYD ARTERIAL EMBOLECTOMY CATHETER?

The FDA 510(k) record lists J-Lloyd Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for J-LLOYD ARTERIAL EMBOLECTOMY CATHETER?

The FDA product code for J-LLOYD ARTERIAL EMBOLECTOMY CATHETER is DXE.

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Other records listing J-Lloyd Medical, Inc. 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.

K973639ELECTRODE SEMI-FLOTATION CATHETER BY J-LLOYD MEDICAL, INC.K971504HEXAPOLAR ELECTRODE BALLOON FLOTATION CATHETERK974335EMBOLECTOMY, IRRIGATION - OCCLUSION BALLOON CATHETER BY J-LLOYD MEDICAL, INC.K974336CHOLANGIOGRAPH BALLOON CATHETER BY J-LLOYD MEDICAL, INC.K963248FLOW DIRECTED THERMODILUTION/INFUSION BALLOON CATHETER (575-110P)K950440DUAL FUNCTION PACING WEDGE PRESSURE BALLOON CATHETER BY J-LLOYD

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Related Devices (Code: DXE)

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.

K240078Fogarty Thru-Lumen Embolectomy CatheterEdwards Lifesciences, LLCK241330Fogarty Fortis Arterial Embolectomy CatheterEdwards LifesciencesK233820Fogarty Arterial Embolectomy Catheter with Gate ValveEdwards LifesciencesK233819Fogarty Venous Thrombectomy CathetersEdwards Lifesciences, LLCK233619Fogarty Corkscrew Catheters; Fogarty Graft Thrombectomy CathetersEdwards LifesciencesK213771Merlin Aspiration SystemMivi Neurovascular, 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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