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FDA 510(k)

Curbell branded Patient Monitoring Cables

K-Number: K182220 · 2018-11-07

Decision Date2018-11-07
Product CodeDSA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Curbell branded Patient Monitoring Cables is a medical device manufactured by Curbell Medical Products, Inc.. It received FDA 510(k) clearance on 2018-11-07 under approval number K182220. 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 Curbell branded Patient Monitoring Cables?

Curbell branded Patient Monitoring Cables is a medical device that received FDA 510(k) clearance on 2018-11-07. It is manufactured by Curbell Medical Products, Inc.. The 510(k) number is K182220.

When was Curbell branded Patient Monitoring Cables approved by the FDA?

Curbell branded Patient Monitoring Cables received FDA 510(k) clearance on 2018-11-07, under approval number K182220.

What company makes Curbell branded Patient Monitoring Cables?

Curbell branded Patient Monitoring Cables is manufactured by Curbell Medical Products, Inc..

What is the FDA product code for Curbell branded Patient Monitoring Cables?

The FDA product code for Curbell branded Patient Monitoring Cables is DSA.

Related Clinical Trials

Related PubMed Literature

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Official Source

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