510(k) K233485

Device
M-Wave
Applicant
Zynex Medical, Inc.
510(k) number
K233485
Product code
IPF
Decision
Substantially Equivalent (SESE)
Decision date
2024-01-26
Date received
2023-10-27
Regulation
890.5850
Classification name
Stimulator, Muscle, Powered
Medical specialty
Physical Medicine
Review panel
Physical Medicine
Device class
2
Clearance type
Abbreviated
Statement or summary
Statement
Third party reviewed
No

Applicant Contact#

Contact
Thomas Sandgaard
Address
9655 Maroon Cir. Englewood CO US 80112 80112

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

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