Citrepore
K-Number: K240450 · 2024-11-06
ApplicantAcuitive Technologies, Inc.
Decision Date2024-11-06
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Citrepore is a medical device manufactured by Acuitive Technologies, Inc.. It received FDA 510(k) clearance on 2024-11-06 under approval number K240450. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Citrepore?
Citrepore is a medical device that received FDA 510(k) clearance on 2024-11-06. It is manufactured by Acuitive Technologies, Inc.. The 510(k) number is K240450.
When was Citrepore approved by the FDA?
Citrepore received FDA 510(k) clearance on 2024-11-06, under approval number K240450.
What company makes Citrepore?
Citrepore is manufactured by Acuitive Technologies, Inc..
What is the FDA product code for Citrepore?
The FDA product code for Citrepore is MQV.
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Related Devices (Code: MQV)
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.