FDA 510(k)

Catheter Clamping Adapter LUER 80369-7, Catheter Clamping Adapter NRFit 80369-7

N.º K: K172777 · 2018-05-03

SolicitantePAJUNK GmbH Medizintechnologie

Fecha de decisión2018-05-03

Código de productoBSO

Comité asesorAN

DecisiónSubstantially Equivalent

Resumen del dispositivo

Catheter Clamping Adapter LUER 80369-7, Catheter Clamping Adapter NRFit 80369-7 is the device name listed in this FDA 510(k) record. The listed applicant is PAJUNK GmbH Medizintechnologie. It received FDA 510(k) clearance on 2018-05-03 under 510(k) number K172777. The device is classified under product code BSO. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Catheter Clamping Adapter LUER 80369-7, Catheter Clamping Adapter NRFit 80369-7?

Catheter Clamping Adapter LUER 80369-7, Catheter Clamping Adapter NRFit 80369-7 is a medical device that received FDA 510(k) clearance on 2018-05-03. The listed applicant is PAJUNK GmbH Medizintechnologie. The 510(k) number is K172777.

When did Catheter Clamping Adapter LUER 80369-7, Catheter Clamping Adapter NRFit 80369-7 receive FDA 510(k) clearance?

Catheter Clamping Adapter LUER 80369-7, Catheter Clamping Adapter NRFit 80369-7 received FDA 510(k) clearance on 2018-05-03, under 510(k) number K172777.

Who is the listed applicant for Catheter Clamping Adapter LUER 80369-7, Catheter Clamping Adapter NRFit 80369-7?

The FDA 510(k) record lists PAJUNK GmbH Medizintechnologie as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Catheter Clamping Adapter LUER 80369-7, Catheter Clamping Adapter NRFit 80369-7?

The FDA product code for Catheter Clamping Adapter LUER 80369-7, Catheter Clamping Adapter NRFit 80369-7 is BSO.

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Otros registros que enlistan a PAJUNK GmbH Medizintechnologie como solicitante

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Fuente oficial

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