K-number	K894723
Device name	SYSTEM 2500 MEDICAL WATERBED
Applicant	Dermanetics Corp.
Product code	IOQ
Device class	Class II
Decision date	Aug 17, 1989
Decision	Substantially Equivalent
Regulation	890.5170

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View the full FDA submission: accessdata.fda.gov

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SYSTEM 2500 MEDICAL WATERBED

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