K-number	K002138
Device name	PARADIGM SILHOUETTE, MODELS MMT-377, 378, 379, 380
Applicant	Maersk Medical A/S
Product code	FPA
Device class	Class II
Decision date	Aug 29, 2000
Decision	Substantially Equivalent
Regulation	880.5440

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View the full FDA submission: accessdata.fda.gov

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PARADIGM SILHOUETTE, MODELS MMT-377, 378, 379, 380

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