PowerPICC Provena Catheters with SOLO Valve Technology
K-Number: K162441 · 2017-04-24
Device Summary
Frequently Asked Questions
What is the PowerPICC Provena Catheters with SOLO Valve Technology?
PowerPICC Provena Catheters with SOLO Valve Technology is a medical device that received FDA 510(k) clearance on 2017-04-24. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K162441.
When did PowerPICC Provena Catheters with SOLO Valve Technology receive FDA 510(k) clearance?
PowerPICC Provena Catheters with SOLO Valve Technology received FDA 510(k) clearance on 2017-04-24, under 510(k) number K162441.
Who is the listed applicant for PowerPICC Provena Catheters with SOLO Valve Technology?
The FDA 510(k) record lists C.R. Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PowerPICC Provena Catheters with SOLO Valve Technology?
The FDA product code for PowerPICC Provena Catheters with SOLO Valve Technology is LJS.
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 C.R. Bard, 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: LJS)
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.