K-number	K011899
Device name	PF 5050 PRESSURE UNIT, MODEL PF 5050
Applicant	Perimed AB
Product code	DPW
Device class	Class II
Decision date	Nov 6, 2001
Decision	Substantially Equivalent
Regulation	870.2100

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View the full FDA submission: accessdata.fda.gov

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PF 5050 PRESSURE UNIT, MODEL PF 5050

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