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FDA 510(k)

Citrepore™

K-Number: K240450 · 2024-11-06

ApplicantAcuitive Technologies, Inc.
Decision Date2024-11-06
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Citrepore™ is the device name listed in this FDA 510(k) record. The listed applicant is Acuitive Technologies, Inc.. It received FDA 510(k) clearance on 2024-11-06 under 510(k) 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. The listed applicant is Acuitive Technologies, Inc.. The 510(k) number is K240450.

When did Citrepore™ receive FDA 510(k) clearance?

Citrepore™ received FDA 510(k) clearance on 2024-11-06, under 510(k) number K240450.

Who is the listed applicant for Citrepore™?

The FDA 510(k) record lists Acuitive Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Citrepore™?

The FDA product code for Citrepore™ is MQV.

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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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