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FDA 510(k)

K100 NEUTRAL DISPLACEMENT NEEDLE FREE CONNECTOR

K-Number: K130023 · 2013-04-03

Decision Date2013-04-03
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

K100 NEUTRAL DISPLACEMENT NEEDLE FREE CONNECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Np Medical, Inc.. It received FDA 510(k) clearance on 2013-04-03 under 510(k) number K130023. 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 K100 NEUTRAL DISPLACEMENT NEEDLE FREE CONNECTOR?

K100 NEUTRAL DISPLACEMENT NEEDLE FREE CONNECTOR is a medical device that received FDA 510(k) clearance on 2013-04-03. The listed applicant is Np Medical, Inc.. The 510(k) number is K130023.

When did K100 NEUTRAL DISPLACEMENT NEEDLE FREE CONNECTOR receive FDA 510(k) clearance?

K100 NEUTRAL DISPLACEMENT NEEDLE FREE CONNECTOR received FDA 510(k) clearance on 2013-04-03, under 510(k) number K130023.

Who is the listed applicant for K100 NEUTRAL DISPLACEMENT NEEDLE FREE CONNECTOR?

The FDA 510(k) record lists Np Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for K100 NEUTRAL DISPLACEMENT NEEDLE FREE CONNECTOR?

The FDA product code for K100 NEUTRAL DISPLACEMENT 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 Np Medical, Inc. 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.

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

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

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