Elecath(R) Transesophageal Pacing Catheter

FDA 510(k) K874154 · Electro-Catheter Corp.

Substantially Equivalent

510(k) numberK874154

Submission

Device name
Elecath(R) Transesophageal Pacing Catheter
Applicant
Electro-Catheter Corp.
Rahway, NJ, US
Received
October 13, 1987
Decision date
April 29, 1988
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KNT – Tubes, Gastrointestinal (And Accessories)
Device class
Class II (moderate risk)
Regulation
21 CFR 876.5980
Specialty
Gastroenterology, Urology

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More from Degania Silicone , Ltd.

510(k)DeviceDecision
K934785MultipaceLDF · Traditional 07/27/1995SE
K943257Tip Deflector (Genesis)DRF · Traditional 04/19/1995SE
K933451Open Tip Multi-Electrode Catheter, ModificationDRF · Traditional 04/19/1995SE
K933450Closed Tip Multi-Electrode Catheter, ModificationDRF · Traditional 04/19/1995SE
K934787Silicore Semi-FloaterLDF · Traditional 02/24/1995SE
K854511Elecath Percutaneous Left Atrial Cannulation SetDQX · Traditional 02/10/1986SE
K854975Elecath Pulsatile Perfusion PumpKFM · Traditional 01/15/1986SE
K850065Elecath Torkfloat Pacing ProbeDTB · Traditional 04/10/1985SE
K850324Elecath Open Tip Bipolar Pacing CatheterLDF · Traditional 03/27/1985SE
K844682Elecath Cardiac Output ComputerDXG · Traditional 03/06/1985SE

Questions and answers

When was Elecath(R) Transesophageal Pacing Catheter cleared by the FDA?

Elecath(R) Transesophageal Pacing Catheter (K874154) received a 510(k) decision of Substantially Equivalent on April 29, 1988, 199 days after the submission was received.

What is the product code of K874154?

The FDA product code is KNT – Tubes, Gastrointestinal (And Accessories), a Class II (moderate risk) device regulated under 21 CFR 876.5980.