K-number	K832703
Device name	ARGON LASER SYS-MODEL 5000
Applicant	Cooper Medical Corp.
Product code	HQE
Device class	Class II
Decision date	Jan 30, 1984
Decision	Substantially Equivalent
Regulation	886.4150

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View the full FDA submission: accessdata.fda.gov

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ARGON LASER SYS-MODEL 5000

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