K-number	K910049
Device name	INTERSPEC APOGEE, MODIFICATION
Applicant	Interspec, Inc.
Product code	DPW
Device class	Class II
Decision date	Apr 29, 1991
Decision	Substantially Equivalent
Regulation	870.2100

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View the full FDA submission: accessdata.fda.gov

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INTERSPEC APOGEE, MODIFICATION

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