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FDA 510(k)

Wattson temporary pacing guidewire (2250)

K-Number: K230637 · 2023-05-05

ApplicantVascular Solutions, LLC
Decision Date2023-05-05
Product CodeDQX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Wattson temporary pacing guidewire (2250) is a medical device manufactured by Vascular Solutions, LLC. It received FDA 510(k) clearance on 2023-05-05 under approval number K230637. The device is classified under product code DQX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Wattson temporary pacing guidewire (2250)?

Wattson temporary pacing guidewire (2250) is a medical device that received FDA 510(k) clearance on 2023-05-05. It is manufactured by Vascular Solutions, LLC. The 510(k) number is K230637.

When was Wattson temporary pacing guidewire (2250) approved by the FDA?

Wattson temporary pacing guidewire (2250) received FDA 510(k) clearance on 2023-05-05, under approval number K230637.

What company makes Wattson temporary pacing guidewire (2250)?

Wattson temporary pacing guidewire (2250) is manufactured by Vascular Solutions, LLC.

What is the FDA product code for Wattson temporary pacing guidewire (2250)?

The FDA product code for Wattson temporary pacing guidewire (2250) is DQX.

Related Clinical Trials

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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.

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