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FDA 510(k)

ELECATH VENTRICULAR PACING WEDGE PRESSURE CATH

K-Number: K844003 · 1984-12-27

ApplicantElectro-Catheter Corp.
Decision Date1984-12-27
Product CodeLDF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ELECATH VENTRICULAR PACING WEDGE PRESSURE CATH is the device name listed in this FDA 510(k) record. The listed applicant is Electro-Catheter Corp.. It received FDA 510(k) clearance on 1984-12-27 under 510(k) number K844003. The device is classified under product code LDF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECATH VENTRICULAR PACING WEDGE PRESSURE CATH?

ELECATH VENTRICULAR PACING WEDGE PRESSURE CATH is a medical device that received FDA 510(k) clearance on 1984-12-27. The listed applicant is Electro-Catheter Corp.. The 510(k) number is K844003.

When did ELECATH VENTRICULAR PACING WEDGE PRESSURE CATH receive FDA 510(k) clearance?

ELECATH VENTRICULAR PACING WEDGE PRESSURE CATH received FDA 510(k) clearance on 1984-12-27, under 510(k) number K844003.

Who is the listed applicant for ELECATH VENTRICULAR PACING WEDGE PRESSURE CATH?

The FDA 510(k) record lists Electro-Catheter Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELECATH VENTRICULAR PACING WEDGE PRESSURE CATH?

The FDA product code for ELECATH VENTRICULAR PACING WEDGE PRESSURE CATH is LDF.

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Other records listing Electro-Catheter Corp. 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.

K934785MULTIPACEK933451OPEN TIP MULTI-ELECTRODE CATHETER, MODIFICATIONK943257TIP DEFLECTOR (GENESIS)K933450CLOSED TIP MULTI-ELECTRODE CATHETER, MODIFICATIONK934787SILICORE SEMI-FLOATERK874154ELECATH(R) TRANSESOPHAGEAL PACING CATHETER

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Related Devices (Code: LDF)

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.

K252042Sync AV II Temporary Pacing CatheterSwift Sync, Inc.K242863Bioptimal Bipolar Pacing CatheterBioptimal International Pte. , Ltd.K251186Bard® Temporary Pacing Electrode Catheter Needle / Cannula (Introducer)C.R. Bard, Inc.K241334Semi-Floating Temporary Pacing Electrode Catheter, Bipolar, Stainless Steel Electrodes, 115 cm, 4Fr. (006221P); Semi-Floating Temporary Pacing Electrode Catheter, Bipolar, Stainless Steel Electrodes, 115 cm, 5Fr. (006225P); Semi-Floating Temporary Pacing Electrode Catheter, Bipolar, Stainless Steel Electrodes, 125 cm, 6Fr. (006241P); Semi-Floating Temporary Pacing Electrode Catheter, Bipolar, Stainless Steel Electrodes, 125 cm, 7Fr. (006242P); NBIH™ Temporary Pacing Electrode Catheter,C.R. Bard, Inc.K241199Rotatable Connector (5944RL)Shenzhen Launch Electrical Co., Ltd.K242705Streamline Unipolar Pediatric Temporary Pacing Lead (6491) Streamline Unipolar Temporary Atrial Pacing Lead (6492) Streamline Unipolar Temporary Myocardial Pacing Wire (6494) Streamline Bipolar Temporary Myocardial Pacing Lead (6495) Streamline Unipolar Temporary Myocardial Pacing Lead (6500)Medtronic, 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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