K-number	K854058
Device name	PK-AC POWERED PATIENT MANUPULATING DEVICE
Applicant	Mannesmann Demag Corp.
Product code	FNG
Device class	Class II
Decision date	Feb 25, 1986
Decision	Substantially Equivalent
Regulation	880.5500

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View the full FDA submission: accessdata.fda.gov

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PK-AC POWERED PATIENT MANUPULATING DEVICE

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