K-number	K133769
Device name	3B RESMART BPAP 25A, BMC RESMART BPAP 25A
Applicant	3B Medical, Inc.
Product code	BZD
Device class	Class II
Decision date	Aug 25, 2014
Decision	Substantially Equivalent
Regulation	868.5905

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View the full FDA submission: accessdata.fda.gov

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3B RESMART BPAP 25A, BMC RESMART BPAP 25A

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