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FDA 510(k)

Reusable Interface Cable 1.5 m (PRD-IFC-002)

K-Number: K242061 · 2024-08-15

ApplicantCreo Medical, Ltd.
Decision Date2024-08-15
Product CodeKNS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Reusable Interface Cable 1.5 m (PRD-IFC-002) is a medical device manufactured by Creo Medical, Ltd.. It received FDA 510(k) clearance on 2024-08-15 under approval number K242061. The device is classified under product code KNS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Reusable Interface Cable 1.5 m (PRD-IFC-002)?

Reusable Interface Cable 1.5 m (PRD-IFC-002) is a medical device that received FDA 510(k) clearance on 2024-08-15. It is manufactured by Creo Medical, Ltd.. The 510(k) number is K242061.

When was Reusable Interface Cable 1.5 m (PRD-IFC-002) approved by the FDA?

Reusable Interface Cable 1.5 m (PRD-IFC-002) received FDA 510(k) clearance on 2024-08-15, under approval number K242061.

What company makes Reusable Interface Cable 1.5 m (PRD-IFC-002)?

Reusable Interface Cable 1.5 m (PRD-IFC-002) is manufactured by Creo Medical, Ltd..

What is the FDA product code for Reusable Interface Cable 1.5 m (PRD-IFC-002)?

The FDA product code for Reusable Interface Cable 1.5 m (PRD-IFC-002) is KNS.

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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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