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FDA 510(k)

Carefusion NeutraClear Needle-free connector

K-Number: K171132 · 2017-07-31

ApplicantCair Lgl
Decision Date2017-07-31
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Carefusion NeutraClear Needle-free connector is the device name listed in this FDA 510(k) record. The listed applicant is Cair Lgl. It received FDA 510(k) clearance on 2017-07-31 under 510(k) number K171132. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Carefusion NeutraClear Needle-free connector?

Carefusion NeutraClear Needle-free connector is a medical device that received FDA 510(k) clearance on 2017-07-31. The listed applicant is Cair Lgl. The 510(k) number is K171132.

When did Carefusion NeutraClear Needle-free connector receive FDA 510(k) clearance?

Carefusion NeutraClear Needle-free connector received FDA 510(k) clearance on 2017-07-31, under 510(k) number K171132.

Who is the listed applicant for Carefusion NeutraClear Needle-free connector?

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

What is the FDA product code for Carefusion NeutraClear Needle-free connector?

The FDA product code for Carefusion NeutraClear Needle-free connector is FPA.

Related Clinical Trials

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.

Other records listing Cair Lgl as applicant

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.

View all 7 devices →

Related Devices (Code: FPA)

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.

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.