ART-Plan
K-Number: K232479 · 2023-12-22
ApplicantTherapanacea
Decision Date2023-12-22
Product CodeMUJ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
ART-Plan is a medical device manufactured by Therapanacea. It received FDA 510(k) clearance on 2023-12-22 under approval number K232479. The device is classified under product code MUJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the ART-Plan?
ART-Plan is a medical device that received FDA 510(k) clearance on 2023-12-22. It is manufactured by Therapanacea. The 510(k) number is K232479.
When was ART-Plan approved by the FDA?
ART-Plan received FDA 510(k) clearance on 2023-12-22, under approval number K232479.
What company makes ART-Plan?
ART-Plan is manufactured by Therapanacea.
What is the FDA product code for ART-Plan?
The FDA product code for ART-Plan is MUJ.
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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.