Filter Purge Line Ec-Fpl Series

FDA 510(k) K833644 · Gish Biomedical, Inc.

Substantially Equivalent

510(k) numberK833644

Submission

Device name
Filter Purge Line Ec-Fpl Series
Applicant
Gish Biomedical, Inc.
Walker, MI, US
Received
October 17, 1983
Decision date
December 29, 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 Filter Purge Line Ec-Fpl Series cleared by the FDA?

Filter Purge Line Ec-Fpl Series (K833644) received a 510(k) decision of Substantially Equivalent on December 29, 1984, 439 days after the submission was received.

What is the product code of K833644?

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