K-number	K924975
Device name	THE ORTHOTRAINER
Applicant	Myofunctional Research Corp. Pty. , Ltd.
Product code	KMY
Device class	Class I
Decision date	Jul 8, 1993
Decision	Substantially Equivalent
Regulation	872.5525

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View the full FDA submission: accessdata.fda.gov

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THE ORTHOTRAINER

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