K-number	K932296
Device name	JR -- OPHTHALMIC ARGON LASER
Applicant	Carson Laserworks
Product code	HQF
Device class	Class II
Decision date	Nov 12, 1993
Decision	Substantially Equivalent
Regulation	886.4390

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View the full FDA submission: accessdata.fda.gov

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JR -- OPHTHALMIC ARGON LASER

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