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FDA 510(k)

VPOD ITPR

K-Number: K172388 · 2017-12-22

ApplicantAdvanced Circulatory System, A Wholly Owned Subsidiary OF
Decision Date2017-12-22
Product CodeBWF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VPOD ITPR is a medical device manufactured by Advanced Circulatory System, A Wholly Owned Subsidiary OF. It received FDA 510(k) clearance on 2017-12-22 under approval number K172388. The device is classified under product code BWF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VPOD ITPR?

VPOD ITPR is a medical device that received FDA 510(k) clearance on 2017-12-22. It is manufactured by Advanced Circulatory System, A Wholly Owned Subsidiary OF. The 510(k) number is K172388.

When was VPOD ITPR approved by the FDA?

VPOD ITPR received FDA 510(k) clearance on 2017-12-22, under approval number K172388.

What company makes VPOD ITPR?

VPOD ITPR is manufactured by Advanced Circulatory System, A Wholly Owned Subsidiary OF.

What is the FDA product code for VPOD ITPR?

The FDA product code for VPOD ITPR is BWF.

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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.

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