510(k) K221257

Device
SpectraWAVE Imaging System
Applicant
Spectrawave, Inc.
510(k) number
K221257
Product code
NQQ
Decision
Substantially Equivalent (SESE)
Decision date
2023-02-28
Date received
2022-05-02
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
Farzad Parsaie
Address
12 Oak Park Dr. Bedford MA US 01730 01730

FDA Registration Numbers

Source Documents

510(k) summary PDF

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