K-number	K840144
Device name	YAG LASER 8000 GASTROINTESTINAL BLEE
Applicant	Cooper Medical Corp.
Product code	FCG
Device class	Class II
Decision date	May 18, 1984
Decision	Substantially Equivalent
Regulation	876.1075

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View the full FDA submission: accessdata.fda.gov

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YAG LASER 8000 GASTROINTESTINAL BLEE

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