K-number	K894788
Device name	DMI SERIES 90 EXAMINATION TABLE
Applicant	M.D. Intl., Inc.
Product code	KMN
Device class	Class I
Decision date	Sep 8, 1989
Decision	Substantially Equivalent
Regulation	880.6140

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View the full FDA submission: accessdata.fda.gov

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DMI SERIES 90 EXAMINATION TABLE

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