Elecath Portal Vein/Biliary Drain Assm

FDA 510(k) K821488 · Electro-Catheter Corp.

Substantially Equivalent

510(k) numberK821488

Submission

Device name
Elecath Portal Vein/Biliary Drain Assm
Applicant
Electro-Catheter Corp.
Mchenry, IL, US
Received
May 18, 1982
Decision date
May 28, 1982
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KNN – Components, Wheelchair
Device class
Class I (low risk)
Regulation
21 CFR 890.3920
Specialty
Physical Medicine

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K925980PMKNN · Traditional Pathfinder Intl. Corp.03/24/1993SE
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K854975Elecath Pulsatile Perfusion PumpKFM · Traditional 01/15/1986SE
K850065Elecath Torkfloat Pacing ProbeDTB · Traditional 04/10/1985SE
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Questions and answers

When was Elecath Portal Vein/Biliary Drain Assm cleared by the FDA?

Elecath Portal Vein/Biliary Drain Assm (K821488) received a 510(k) decision of Substantially Equivalent on May 28, 1982, 10 days after the submission was received.

What is the product code of K821488?

The FDA product code is KNN – Components, Wheelchair, a Class I (low risk) device regulated under 21 CFR 890.3920.