K-number	K943969
Device name	MODEL 578 MOBILE SURGICAL STRETCHER
Applicant	Hausted, Inc.
Product code	FPO
Device class	Class II
Decision date	Jan 25, 1995
Decision	Substantially Equivalent
Regulation	880.6910

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View the full FDA submission: accessdata.fda.gov

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MODEL 578 MOBILE SURGICAL STRETCHER

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