K-number	K870819
Device name	BUBBLE TRAP CAT. NO. B-180
Applicant	American Omni Medical, Inc.
Product code	DWF
Device class	Class II
Decision date	Jun 8, 1987
Decision	Substantially Equivalent
Regulation	870.4210

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View the full FDA submission: accessdata.fda.gov

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BUBBLE TRAP CAT. NO. B-180

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