K-number	K030396
Device name	OMNI~NEB; OMNI~MAX
Applicant	B&B Medical Technologies, Inc.
Product code	CAF
Device class	Class II
Decision date	May 7, 2004
Decision	Substantially Equivalent
Regulation	868.5630

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View the full FDA submission: accessdata.fda.gov

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OMNI~NEB; OMNI~MAX

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