EVAC
K-Number: K243205 · 2025-06-03
ApplicantPhasor Health, LLC
Decision Date2025-06-03
Product CodeJXG
Advisory CommitteeNE
DecisionSubstantially Equivalent
Device Summary
EVAC is a medical device manufactured by Phasor Health, LLC. It received FDA 510(k) clearance on 2025-06-03 under approval number K243205. The device is classified under product code JXG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the EVAC?
EVAC is a medical device that received FDA 510(k) clearance on 2025-06-03. It is manufactured by Phasor Health, LLC. The 510(k) number is K243205.
When was EVAC approved by the FDA?
EVAC received FDA 510(k) clearance on 2025-06-03, under approval number K243205.
What company makes EVAC?
EVAC is manufactured by Phasor Health, LLC.
What is the FDA product code for EVAC?
The FDA product code for EVAC is JXG.
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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.