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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 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.

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. 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.

Other records listing PAJUNK GmbH Medizintechnologie as applicant

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Related Devices (Code: BSO)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K241410EDEN ControlCathJmt Co., Ltd.K231242Perifix FX Catheter; Contiplex FX CatheterB.Braun Medical, Inc.K230603Arrow Non-Stimulating SnapLock Adapter (K-05520-005C); Arrow Non-Stimulating Next Gen SnapLock Adapter (Luer Connection) (CA-000010-19); Arrow Non-Stimulating Next Gen SnapLock Adapter (Neuraxial Connection) (CA-000014-19); Arrow Stimulating SnapLock Adapter (with cable) (TZ-02060-001); Arrow Stimulating SnapLock Adapter (with tab) (TZ-05000-002)Teleflex MedicalK193664SubQKath Catheter and Needle SetHk SurgicalK200624Percutaneous IntroducerEpimed International, Inc.K191470C-CAT Anaesthesia Catheter kitCimpax Aps

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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