K-number	K812628
Device name	ACA FIBRINOGEN CALIBRATOR
Applicant	E.I. Dupont DE Nemours & Co., Inc.
Product code	GFX
Device class	Class II
Decision date	Nov 24, 1981
Decision	Substantially Equivalent
Regulation	864.7340

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View the full FDA submission: accessdata.fda.gov

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ACA FIBRINOGEN CALIBRATOR

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