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Recognized a 510(k)/PMA number — showing its clearance record and devices.

Clearance record K240450

Citrepore™ · Acuitive Technologies, Inc. · decided 2024-11-06 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
6cc Citregraft Cylinder36-106-0005Acuitive Technologies, Inc.MQV00810027272300
12.5cc Citregraft Cylinder36-106-0006Acuitive Technologies, Inc.MQV00810027272317
3cc Citregraft Cylinder36-106-0004Acuitive Technologies, Inc.MQV00810027272294