K-number	K092685
Device name	PNEUMOTHERML, MODEL: 5800
Applicant	Salter Labs
Product code	BZQ
Device class	Class II
Decision date	Nov 24, 2009
Decision	Substantially Equivalent
Regulation	868.2375

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View the full FDA submission: accessdata.fda.gov

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PNEUMOTHERML, MODEL: 5800

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