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FDA 510(k)

Reprocessed ViewFlex Xtra ICE Catheter (D087031)

K-Number: K231621 · 2023-07-25

Decision Date2023-07-25
Product CodeOWQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Reprocessed ViewFlex Xtra ICE Catheter (D087031) is a medical device manufactured by Stryker Sustainability Solutions. It received FDA 510(k) clearance on 2023-07-25 under approval number K231621. The device is classified under product code OWQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Reprocessed ViewFlex Xtra ICE Catheter (D087031)?

Reprocessed ViewFlex Xtra ICE Catheter (D087031) is a medical device that received FDA 510(k) clearance on 2023-07-25. It is manufactured by Stryker Sustainability Solutions. The 510(k) number is K231621.

When was Reprocessed ViewFlex Xtra ICE Catheter (D087031) approved by the FDA?

Reprocessed ViewFlex Xtra ICE Catheter (D087031) received FDA 510(k) clearance on 2023-07-25, under approval number K231621.

What company makes Reprocessed ViewFlex Xtra ICE Catheter (D087031)?

Reprocessed ViewFlex Xtra ICE Catheter (D087031) is manufactured by Stryker Sustainability Solutions.

What is the FDA product code for Reprocessed ViewFlex Xtra ICE Catheter (D087031)?

The FDA product code for Reprocessed ViewFlex Xtra ICE Catheter (D087031) is OWQ.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.