Jehle Coronary Perfusion Catheters

FDA 510(k) K884946 · Pilling Co.

Substantially Equivalent

510(k) numberK884946

Submission

Device name
Jehle Coronary Perfusion Catheters
Applicant
Pilling Co.
Fort Washington, PA, US
Received
November 28, 1988
Decision date
February 6, 1989
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KRA – Catheter, Continuous Flush
Device class
Class II (moderate risk)
Regulation
21 CFR 870.1210
Specialty
Cardiovascular

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K231279Peregrine System Infusion Catheter 4-7 mm, Peregrine System Infusion Catheter 3-4 mmKRA · Traditional Ablative Solutions, Inc.07/05/2023SE
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Questions and answers

When was Jehle Coronary Perfusion Catheters cleared by the FDA?

Jehle Coronary Perfusion Catheters (K884946) received a 510(k) decision of Substantially Equivalent on February 6, 1989, 70 days after the submission was received.

What is the product code of K884946?

The FDA product code is KRA – Catheter, Continuous Flush, a Class II (moderate risk) device regulated under 21 CFR 870.1210.