NAC PLUS NEEDLELESS ACCESS CONNECTOR
K-Number: K011193 · 2001-06-12
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Device Summary
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
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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