FDA 510(k)

TransFix/EDTA Vacuum Blood Collection Tubes

N.º K: K162723 · 2017-06-22

Fecha de decisión2017-06-22

Código de productoGIM

Comité asesorCH

DecisiónSubstantially Equivalent

Resumen del dispositivo

TransFix/EDTA Vacuum Blood Collection Tubes is the device name listed in this FDA 510(k) record. The listed applicant is Caltag Medsystems, Ltd.. It received FDA 510(k) clearance on 2017-06-22 under 510(k) number K162723. The device is classified under product code GIM. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the TransFix/EDTA Vacuum Blood Collection Tubes?

TransFix/EDTA Vacuum Blood Collection Tubes is a medical device that received FDA 510(k) clearance on 2017-06-22. The listed applicant is Caltag Medsystems, Ltd.. The 510(k) number is K162723.

When did TransFix/EDTA Vacuum Blood Collection Tubes receive FDA 510(k) clearance?

TransFix/EDTA Vacuum Blood Collection Tubes received FDA 510(k) clearance on 2017-06-22, under 510(k) number K162723.

Who is the listed applicant for TransFix/EDTA Vacuum Blood Collection Tubes?

The FDA 510(k) record lists Caltag Medsystems, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TransFix/EDTA Vacuum Blood Collection Tubes?

The FDA product code for TransFix/EDTA Vacuum Blood Collection Tubes is GIM.

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Fuente oficial

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