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FDA 510(k)

VPOD ITPR

K-Number: K172388 · 2017-12-22

Decision Date2017-12-22
Product CodeBWF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VPOD ITPR is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Circulatory System, A Wholly Owned Subsidiary OF. It received FDA 510(k) clearance on 2017-12-22 under 510(k) 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. The listed applicant is Advanced Circulatory System, A Wholly Owned Subsidiary OF. The 510(k) number is K172388.

When did VPOD ITPR receive FDA 510(k) clearance?

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

Who is the listed applicant for VPOD ITPR?

The FDA 510(k) record lists Advanced Circulatory System, A Wholly Owned Subsidiary OF as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VPOD ITPR?

The FDA product code for VPOD ITPR is BWF.

Related Devices (Code: BWF)

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

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