FDA 510(k)

BD Prevue II Peripheral Vascular Access System

K-Number: K240146 · 2024-02-18

Decision Date2024-02-18

Product CodeIYO

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

BD Prevue II Peripheral Vascular Access System is a medical device manufactured by Bard Access Systems, Inc.. It received FDA 510(k) clearance on 2024-02-18 under approval number K240146. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BD Prevue II Peripheral Vascular Access System?

BD Prevue II Peripheral Vascular Access System is a medical device that received FDA 510(k) clearance on 2024-02-18. It is manufactured by Bard Access Systems, Inc.. The 510(k) number is K240146.

When was BD Prevue II Peripheral Vascular Access System approved by the FDA?

BD Prevue II Peripheral Vascular Access System received FDA 510(k) clearance on 2024-02-18, under approval number K240146.

What company makes BD Prevue II Peripheral Vascular Access System?

BD Prevue II Peripheral Vascular Access System is manufactured by Bard Access Systems, Inc..

What is the FDA product code for BD Prevue II Peripheral Vascular Access System?

The FDA product code for BD Prevue II Peripheral Vascular Access System is IYO.

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Other Devices by Bard Access Systems, Inc.

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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.