Intraluminal Applicator Set
K-Number: K242961 · 2024-11-26
ApplicantVarian Medical Systems
Decision Date2024-11-26
Product CodeJAQ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Intraluminal Applicator Set is a medical device manufactured by Varian Medical Systems. It received FDA 510(k) clearance on 2024-11-26 under approval number K242961. The device is classified under product code JAQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Intraluminal Applicator Set?
Intraluminal Applicator Set is a medical device that received FDA 510(k) clearance on 2024-11-26. It is manufactured by Varian Medical Systems. The 510(k) number is K242961.
When was Intraluminal Applicator Set approved by the FDA?
Intraluminal Applicator Set received FDA 510(k) clearance on 2024-11-26, under approval number K242961.
What company makes Intraluminal Applicator Set?
Intraluminal Applicator Set is manufactured by Varian Medical Systems.
What is the FDA product code for Intraluminal Applicator Set?
The FDA product code for Intraluminal Applicator Set is JAQ.
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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.