K-number	K102229
Device name	PULMOTRACK 2020 SYSTEM
Applicant	Karmelsonix
Product code	BZM
Device class	Class II
Decision date	Mar 4, 2011
Decision	Substantially Equivalent
Regulation	868.1900

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View the full FDA submission: accessdata.fda.gov

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PULMOTRACK 2020 SYSTEM

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