Adapter-Y Type/Coronary Perfusion

FDA 510(k) K791498 · Dlp, Inc.

Substantially Equivalent

510(k) numberK791498

Submission

Device name
Adapter-Y Type/Coronary Perfusion
Applicant
Dlp, Inc.
Mchenry, IL, US
Received
August 2, 1979
Decision date
August 28, 1979
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 Adapter-Y Type/Coronary Perfusion cleared by the FDA?

Adapter-Y Type/Coronary Perfusion (K791498) received a 510(k) decision of Substantially Equivalent on August 28, 1979, 26 days after the submission was received.

What is the product code of K791498?

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