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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 the device name listed in this FDA 510(k) record. The listed applicant is Creo Medical, Ltd.. It received FDA 510(k) clearance on 2024-08-15 under 510(k) 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. The listed applicant is Creo Medical, Ltd.. The 510(k) number is K242061.

When did Reusable Interface Cable 1.5 m (PRD-IFC-002) receive FDA 510(k) clearance?

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

Who is the listed applicant for Reusable Interface Cable 1.5 m (PRD-IFC-002)?

The FDA 510(k) record lists Creo Medical, Ltd. as the applicant. This does not by itself establish the device manufacturer.

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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