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FDA 510(k)

Fogg System Patient Monitoring Cables

K-Number: K222712 · 2023-11-22

ApplicantFogg System Company, Inc.
Decision Date2023-11-22
Product CodeDSA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Fogg System Patient Monitoring Cables is a medical device manufactured by Fogg System Company, Inc.. It received FDA 510(k) clearance on 2023-11-22 under approval number K222712. 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 Fogg System Patient Monitoring Cables?

Fogg System Patient Monitoring Cables is a medical device that received FDA 510(k) clearance on 2023-11-22. It is manufactured by Fogg System Company, Inc.. The 510(k) number is K222712.

When was Fogg System Patient Monitoring Cables approved by the FDA?

Fogg System Patient Monitoring Cables received FDA 510(k) clearance on 2023-11-22, under approval number K222712.

What company makes Fogg System Patient Monitoring Cables?

Fogg System Patient Monitoring Cables is manufactured by Fogg System Company, Inc..

What is the FDA product code for Fogg System Patient Monitoring Cables?

The FDA product code for Fogg System Patient Monitoring Cables is DSA.

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Related PubMed Literature

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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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