K-number	K930784
Device name	THE DE SOUTTER M193 REAMER
Applicant	De Soutter Medical, Ltd.
Product code	HSZ
Device class	Class I
Decision date	Oct 27, 1993
Decision	Substantially Equivalent
Regulation	878.4820

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View the full FDA submission: accessdata.fda.gov

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THE DE SOUTTER M193 REAMER

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