510(k) K871472

Device
KINESTIM MUSCLE STIMULATOR
Applicant
PROMATEK INDUSTRIES, LTD.
510(k) number
K871472
Product code
IPF  
Decision
Substantially Equivalent For Some Indications (SN)
Decision date
1987-06-29
Date received
1987-04-14
Regulation
890.5850
Classification name
Stimulator, Muscle, Powered
Medical specialty
Physical Medicine
Review panel
Physical Medicine
Device class
2
Clearance type
Traditional
Third party reviewed
No

Related Records

Applicant Contact

Contact
ART LEVINE
Address
8390 Mayrand, Montreal Quebec, H4p 2c9 CA

FDA Registration Numbers

Source Documents

510(k) summary PDF not indicated by FDA

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Legacy Summary

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FDA Review

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