Disposable Quick Release Perfusion Adap

FDA 510(k) K802544 · Texas Medical Products, Inc.

Substantially Equivalent

510(k) numberK802544

Submission

Device name
Disposable Quick Release Perfusion Adap
Applicant
Texas Medical Products, Inc.
Mchenry, IL, US
Received
October 15, 1980
Decision date
January 16, 1981
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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K140475Rotating AdaptersDTL · Traditional Merit Medical Systems, Inc.04/16/2014SE
K131124ColignDTL · Traditional Jilin Coronado Medical , Ltd.08/28/2013SE
K123448Affinity Flexible Luer Lock Adapter with Balance Biosurface, Affinity Flexible Luer Lock…DTL · Special Medtronic, Inc.12/13/2012SE
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K122301Guardian II Hemostasis Valve Guardian II NC Hemostasis ValveDTL · Traditional Vascular Solutions Zerusa , Ltd.09/07/2012SE
K120069Medline Stopcock and ManifoldDTL · Traditional Medline Industries, Inc.04/03/2012SE
K113148E-PassDTL · Traditional Synexmed(Shenzhen)Company Limited02/28/2012SE
K113845Tubing, Conmnectors, and Accessories Wit Balance BiosurfaceDTL · Special Medtronic, Inc.01/25/2012SE

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K851575Dr. Bruno Lnage Mini Photometer · Traditional 10/18/1985SE
K830634Cardiotomy FilterJOD · Traditional 06/30/1983SE
K813587Disposable Thoracic CatheterGBS · Traditional 01/12/1982SE
K810532Disposable StopcockDTZ · Traditional 04/23/1981SE
K810515Disposable 2-STAGE CannulaDWF · Traditional 04/23/1981SE
K810395Pre-Bypass FilterKRJ · Traditional 03/05/1981SE
K802545Cardioplegic SetsDTR · Traditional 01/16/1981SE
K802543Ridgid Vena Cava CannulaeDWF · Traditional 01/16/1981SE

Questions and answers

When was Disposable Quick Release Perfusion Adap cleared by the FDA?

Disposable Quick Release Perfusion Adap (K802544) received a 510(k) decision of Substantially Equivalent on January 16, 1981, 93 days after the submission was received.

What is the product code of K802544?

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