510(k) K223802

Device
accufit
Applicant
Mettler Electronics Corporation
510(k) number
K223802
Product code
IPF
Decision
Substantially Equivalent (SESE)
Decision date
2023-10-06
Date received
2022-12-19
Regulation
890.5850
Classification name
Stimulator, Muscle, Powered
Medical specialty
Physical Medicine
Review panel
Physical Medicine
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
An Le
Address
1333 S. Claudina St. Anaheim CA US 92805 92805

FDA Registration Numbers

Source Documents

510(k) summary PDF

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