K-number	K781104
Device name	PLASMA COAGULATION CONT., ABNORMAL
Applicant	Ortho Diagnostics, Inc.
Product code	GFO
Device class	Class II
Decision date	Aug 10, 1978
Decision	Substantially Equivalent
Regulation	864.7925

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View the full FDA submission: accessdata.fda.gov

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PLASMA COAGULATION CONT., ABNORMAL

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