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FDA 510(k)

NAC PLUS NEEDLELESS ACCESS CONNECTOR

K-Number: K011193 · 2001-06-12

Decision Date2001-06-12
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NAC PLUS NEEDLELESS ACCESS CONNECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Porex Medical Products. It received FDA 510(k) clearance on 2001-06-12 under 510(k) number K011193. 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 NAC PLUS NEEDLELESS ACCESS CONNECTOR?

NAC PLUS NEEDLELESS ACCESS CONNECTOR is a medical device that received FDA 510(k) clearance on 2001-06-12. The listed applicant is Porex Medical Products. The 510(k) number is K011193.

When did NAC PLUS NEEDLELESS ACCESS CONNECTOR receive FDA 510(k) clearance?

NAC PLUS NEEDLELESS ACCESS CONNECTOR received FDA 510(k) clearance on 2001-06-12, under 510(k) number K011193.

Who is the listed applicant for NAC PLUS NEEDLELESS ACCESS CONNECTOR?

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

What is the FDA product code for NAC PLUS NEEDLELESS ACCESS CONNECTOR?

The FDA product code for NAC PLUS NEEDLELESS ACCESS 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.

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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