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FDA 510(k)

Caretaker Platform, VitalStream Platform, CT5

K-Number: K211588 · 2021-08-13

ApplicantCaretaker Medical
Decision Date2021-08-13
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Caretaker Platform, VitalStream Platform, CT5 is a medical device manufactured by Caretaker Medical. It received FDA 510(k) clearance on 2021-08-13 under approval number K211588. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Caretaker Platform, VitalStream Platform, CT5?

Caretaker Platform, VitalStream Platform, CT5 is a medical device that received FDA 510(k) clearance on 2021-08-13. It is manufactured by Caretaker Medical. The 510(k) number is K211588.

When was Caretaker Platform, VitalStream Platform, CT5 approved by the FDA?

Caretaker Platform, VitalStream Platform, CT5 received FDA 510(k) clearance on 2021-08-13, under approval number K211588.

What company makes Caretaker Platform, VitalStream Platform, CT5?

Caretaker Platform, VitalStream Platform, CT5 is manufactured by Caretaker Medical.

What is the FDA product code for Caretaker Platform, VitalStream Platform, CT5?

The FDA product code for Caretaker Platform, VitalStream Platform, CT5 is DXN.

Other Devices by Caretaker Medical

K251275VitalStream ART Connect; VitalStream-Hemo

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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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