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FDA 510(k)

PCA-C1 series Patient Cable

K-Number: K200722 · 2021-06-03

ApplicantQT Medical, Inc.
Decision Date2021-06-03
Product CodeDSA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PCA-C1 series Patient Cable is a medical device manufactured by QT Medical, Inc.. It received FDA 510(k) clearance on 2021-06-03 under approval number K200722. The device is classified under product code DSA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PCA-C1 series Patient Cable?

PCA-C1 series Patient Cable is a medical device that received FDA 510(k) clearance on 2021-06-03. It is manufactured by QT Medical, Inc.. The 510(k) number is K200722.

When was PCA-C1 series Patient Cable approved by the FDA?

PCA-C1 series Patient Cable received FDA 510(k) clearance on 2021-06-03, under approval number K200722.

What company makes PCA-C1 series Patient Cable?

PCA-C1 series Patient Cable is manufactured by QT Medical, Inc..

What is the FDA product code for PCA-C1 series Patient Cable?

The FDA product code for PCA-C1 series Patient Cable is DSA.

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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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