FDA.report

510(k) K231575

Device
Vecttor VT-300
Applicant
Artaflex, Inc.
510(k) number
K231575
Product code
LIH
Decision
Substantially Equivalent (SESE)
Decision date
2024-02-08
Date received
2023-05-31
Regulation
882.5890
Classification name
Interferential Current Therapy
Medical specialty
Neurology
Review panel
Neurology
Device class
2
Clearance type
Abbreviated
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Gerry Iuliano
Address
181 Whitehall Dr. Markham CA L3T 9T1 L3T 9T1

FDA Registration Numbers

Source Documents

510(k) summary PDF

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