K-number	K962903
Device name	PRESTIGE MEDICAL SERIES 2100 CLINICAL AUTOCLAVE
Applicant	Prestige Medical Corp.
Product code	FLE
Device class	Class II
Decision date	Mar 3, 1998
Decision	Substantially Equivalent
Regulation	880.6880

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View the full FDA submission: accessdata.fda.gov

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PRESTIGE MEDICAL SERIES 2100 CLINICAL AUTOCLAVE

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