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FDA 510(k)

ELECTRODE SEMI-FLOTATION CATHETER BY J-LLOYD MEDICAL, INC.

K-Number: K973639 · 1998-04-20

ApplicantJ-Lloyd Medical, Inc.
Decision Date1998-04-20
Product CodeDRF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ELECTRODE SEMI-FLOTATION CATHETER BY J-LLOYD MEDICAL, INC. 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 1998-04-20 under 510(k) number K973639. The device is classified under product code DRF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTRODE SEMI-FLOTATION CATHETER BY J-LLOYD MEDICAL, INC.?

ELECTRODE SEMI-FLOTATION CATHETER BY J-LLOYD MEDICAL, INC. is a medical device that received FDA 510(k) clearance on 1998-04-20. The listed applicant is J-Lloyd Medical, Inc.. The 510(k) number is K973639.

When did ELECTRODE SEMI-FLOTATION CATHETER BY J-LLOYD MEDICAL, INC. receive FDA 510(k) clearance?

ELECTRODE SEMI-FLOTATION CATHETER BY J-LLOYD MEDICAL, INC. received FDA 510(k) clearance on 1998-04-20, under 510(k) number K973639.

Who is the listed applicant for ELECTRODE SEMI-FLOTATION CATHETER BY J-LLOYD MEDICAL, INC.?

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 ELECTRODE SEMI-FLOTATION CATHETER BY J-LLOYD MEDICAL, INC.?

The FDA product code for ELECTRODE SEMI-FLOTATION CATHETER BY J-LLOYD MEDICAL, INC. is DRF.

Related Clinical Trials

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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.

K971504HEXAPOLAR ELECTRODE BALLOON FLOTATION CATHETERK974336CHOLANGIOGRAPH BALLOON CATHETER BY J-LLOYD MEDICAL, INC.K974335EMBOLECTOMY, IRRIGATION - OCCLUSION BALLOON CATHETER BY J-LLOYD MEDICAL, INC.K963248FLOW DIRECTED THERMODILUTION/INFUSION BALLOON CATHETER (575-110P)K950440DUAL FUNCTION PACING WEDGE PRESSURE BALLOON CATHETER BY J-LLOYDK940547FLOW DIRECT THERMODILUT BALLOON CATH HEPARIN COATED

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Related Devices (Code: DRF)

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.

K252794Vision-MR™ Diagnostic CatheterImricor Medical Systems, Inc.K250590MAGiC Sweep™ EP Mapping CatheterStereotaxis, Inc.K250310VIKING™ Fixed Curve Diagnostic CatheterBoston Scientific CorporationK240366EP•XT™ Unidirectional Steerable Diagnostic Catheter; Dynamic Tip™ Unidirectional Steerable Diagnostic Catheter; Dynamic XT™ Unidirectional Steerable Diagnostic CatheterBoston Scientific CorporationK233900Nordica PV Cryo Mapping CatheterSynaptic Medical CorporationK233397Cosine-10TM Diagnostic CatheterMedtronic, 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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