PLEURX PLEURAL CATHETER SYSTEMS
K-Number: K112831 · 2012-02-16
Advertisement
Device Summary
Frequently Asked Questions
What is the PLEURX PLEURAL CATHETER SYSTEMS?
PLEURX PLEURAL CATHETER SYSTEMS is a medical device that received FDA 510(k) clearance on 2012-02-16. The listed applicant is Care Fusion. The 510(k) number is K112831.
When did PLEURX PLEURAL CATHETER SYSTEMS receive FDA 510(k) clearance?
PLEURX PLEURAL CATHETER SYSTEMS received FDA 510(k) clearance on 2012-02-16, under 510(k) number K112831.
Who is the listed applicant for PLEURX PLEURAL CATHETER SYSTEMS?
The FDA 510(k) record lists Care Fusion as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PLEURX PLEURAL CATHETER SYSTEMS?
The FDA product code for PLEURX PLEURAL CATHETER SYSTEMS is DWM.
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 Care Fusion 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: DWM)
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.
Advertisement