CENTRIX NEEDLETUBE
K-Number: K882651 · 1988-08-10
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Device Summary
Frequently Asked Questions
What is the CENTRIX NEEDLETUBE?
CENTRIX NEEDLETUBE is a medical device that received FDA 510(k) clearance on 1988-08-10. The listed applicant is Centrix, Inc.. The 510(k) number is K882651.
When did CENTRIX NEEDLETUBE receive FDA 510(k) clearance?
CENTRIX NEEDLETUBE received FDA 510(k) clearance on 1988-08-10, under 510(k) number K882651.
Who is the listed applicant for CENTRIX NEEDLETUBE?
The FDA 510(k) record lists Centrix, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CENTRIX NEEDLETUBE?
The FDA product code for CENTRIX NEEDLETUBE is EKJ.
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 Centrix, 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: EKJ)
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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