K-number	K864503
Device name	MODIFIED RLV-2100 B
Applicant	American Omni Medical, Inc.
Product code	DWD
Device class	Class II
Decision date	Jan 6, 1987
Decision	Substantially Equivalent
Regulation	870.4430

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View the full FDA submission: accessdata.fda.gov

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MODIFIED RLV-2100 B

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