K-number	K852439
Device name	FETA SCAN 1000 OBSTETRICAL IMAGER
Applicant	International Biomedics, Inc.
Product code	HEM
Device class	Class II
Decision date	Aug 30, 1985
Decision	Substantially Equivalent
Regulation	884.2225

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View the full FDA submission: accessdata.fda.gov

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FETA SCAN 1000 OBSTETRICAL IMAGER

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