K-number	K812637
Device name	ACMI BIPOLAR HEMOSTATIC SOURCE
Applicant	American Cystocope Makers, Inc.
Product code	GEI
Device class	Class II
Decision date	Oct 26, 1981
Decision	Substantially Equivalent
Regulation	878.4400

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Source

View the full FDA submission: accessdata.fda.gov

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ACMI BIPOLAR HEMOSTATIC SOURCE

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