MODIFICATION TO THE NAC PLUS NEEDLELESS ACCESS CONNECTOR
K-Number: K041179 · 2004-06-04
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Device Summary
Frequently Asked Questions
What is the MODIFICATION TO THE NAC PLUS NEEDLELESS ACCESS CONNECTOR?
MODIFICATION TO THE NAC PLUS NEEDLELESS ACCESS CONNECTOR is a medical device that received FDA 510(k) clearance on 2004-06-04. The listed applicant is Medegen Medical Manufacturing Services, Inc.. The 510(k) number is K041179.
When did MODIFICATION TO THE NAC PLUS NEEDLELESS ACCESS CONNECTOR receive FDA 510(k) clearance?
MODIFICATION TO THE NAC PLUS NEEDLELESS ACCESS CONNECTOR received FDA 510(k) clearance on 2004-06-04, under 510(k) number K041179.
Who is the listed applicant for MODIFICATION TO THE NAC PLUS NEEDLELESS ACCESS CONNECTOR?
The FDA 510(k) record lists Medegen Medical Manufacturing Services, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODIFICATION TO THE NAC PLUS NEEDLELESS ACCESS CONNECTOR?
The FDA product code for MODIFICATION TO THE 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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