Arterial Filter Purge Line W/Check Valv

FDA 510(k) K840603 · Shiley, Inc.

Substantially Equivalent

510(k) numberK840603

Submission

Device name
Arterial Filter Purge Line W/Check Valv
Applicant
Shiley, Inc.
Mchenry, IL, US
Received
February 10, 1984
Decision date
April 19, 1984
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DTL – Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass
Device class
Class II (moderate risk)
Regulation
21 CFR 870.4290
Specialty
Cardiovascular

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Questions and answers

When was Arterial Filter Purge Line W/Check Valv cleared by the FDA?

Arterial Filter Purge Line W/Check Valv (K840603) received a 510(k) decision of Substantially Equivalent on April 19, 1984, 69 days after the submission was received.

What is the product code of K840603?

The FDA product code is DTL – Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass, a Class II (moderate risk) device regulated under 21 CFR 870.4290.