K-number	K852422
Device name	MODEL 500 PEDIATRIC STRETCHER/CRIB
Applicant	Midmark Corp.
Product code	FMS
Device class	Class II
Decision date	Jul 5, 1985
Decision	Substantially Equivalent
Regulation	880.5140

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View the full FDA submission: accessdata.fda.gov

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MODEL 500 PEDIATRIC STRETCHER/CRIB

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