K-number	K951901
Device name	MASTERSCREEN PFT BODY
Applicant	Erich Jaeger GmbH & Co. KG
Product code	JEH
Device class	Class II
Decision date	Jul 31, 1995
Decision	Substantially Equivalent
Regulation	868.1760

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View the full FDA submission: accessdata.fda.gov

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MASTERSCREEN PFT BODY

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