MARK V HIGH VOLTAGE GALVANIC STIMULATORR

Stimulator, Muscle, Powered

ORTHION CORP.

The following data is part of a premarket notification filed by Orthion Corp. with the FDA for Mark V High Voltage Galvanic Stimulatorr.

Pre-market Notification Details

Device IDK832546
510k NumberK832546
Device Name:MARK V HIGH VOLTAGE GALVANIC STIMULATORR
ClassificationStimulator, Muscle, Powered
Applicant ORTHION CORP. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeIPF  
CFR Regulation Number890.5850 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1983-07-29
Decision Date1983-10-14

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.