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FDA 510(k)

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

K-Number: K172777 · 2018-05-03

ApplicantPAJUNK GmbH Medizintechnologie
Decision Date2018-05-03
Product CodeBSO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

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

Frequently Asked Questions

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. It is manufactured by PAJUNK GmbH Medizintechnologie. The 510(k) number is K172777.

When was Catheter Clamping Adapter LUER 80369-7, Catheter Clamping Adapter NRFit 80369-7 approved by the FDA?

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

What company makes 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 manufactured by PAJUNK GmbH Medizintechnologie.

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.

Related Clinical Trials

NCT04498598 Structural Modification In Supraglottic Airway Device RECRUITING

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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