510(k) K251730

Device
LIA Console (542-7)
Applicant
Leadoptik, Inc.
510(k) number
K251730
Product code
NQQ
Decision
Substantially Equivalent (SESE)
Decision date
2025-12-19
Date received
2025-06-06
Regulation
892.1560
Classification name
System, Imaging, Optical Coherence Tomography (Oct)
Medical specialty
Radiology
Review panel
Radiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
Mohammadreza Khorasaninejad
Address
2380 Qume Dr. Suite A San Jose CA US 95131 95131

FDA Registration Numbers

Source Documents

510(k) summary PDF

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