Ibc Cardiac Suction Ward

FDA 510(k) K963756 · International Biophysics Corp.

Substantially Equivalent

510(k) numberK963756

Submission

Device name
Ibc Cardiac Suction Ward
Applicant
International Biophysics Corp.
Austin, TX, US
Received
September 17, 1996
Decision date
November 14, 1997
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
DTS – Sucker, Cardiotomy Return, Cardiopulmonary Bypass
Device class
Class II (moderate risk)
Regulation
21 CFR 870.4420
Specialty
Cardiovascular

Other 510(k)s with product code DTS

510(k)DeviceApplicantDecision
K053021Estech Clearview MV Atrial DepressorDTS · Traditional Estech, Inc.01/26/2006SE
K982891California Medical Laboratories Inc. Standard and Small Rigid Tip Suction WandsDTS · Traditional California Medical Laboratories, Inc.09/30/1998SE
K905008Flexible Intracardiac Suction DeviceDTS · Traditional Gish Biomedical, Inc.01/23/1991SE
K900339Hand-Held Intracardiac Suckers W/Ergonomic HandlesDTS · Traditional Shiley, Inc.03/28/1990SE
K891906Robicsek Intracardiac Suction WandDTS · Traditional Gish Biomedical, Inc.06/13/1989SE
K801641Ohio Disposable Clear Suction InstrumentDTS · Traditional Ohio Medical Products07/28/1980SE
K801400Disposable Sucker SystemDTS · Traditional Texas Medical Products, Inc.06/30/1980SE
K791846Dispossable Suction Tube, 6 FrenchDTS · Traditional Dlp, Inc.10/02/1979SE

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Questions and answers

When was Ibc Cardiac Suction Ward cleared by the FDA?

Ibc Cardiac Suction Ward (K963756) received a 510(k) decision of Substantially Equivalent on November 14, 1997, 423 days after the submission was received.

What is the product code of K963756?

The FDA product code is DTS – Sucker, Cardiotomy Return, Cardiopulmonary Bypass, a Class II (moderate risk) device regulated under 21 CFR 870.4420.