K-number	K800223
Device name	PATIENT POSITIONING SYSTEM 1D OR 2D
Applicant	Laboratoire National D'Essais
Product code	IWE
Device class	Class I
Decision date	Mar 3, 1980
Decision	Substantially Equivalent
Regulation	892.5780

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Source

View the full FDA submission: accessdata.fda.gov

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PATIENT POSITIONING SYSTEM 1D OR 2D

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