K-number	K853432
Device name	5.0 IOP & 7.5 IOP PROBES
Applicant	Diasonics, Inc.
Product code	GXW
Device class	Class II
Decision date	Feb 7, 1986
Decision	Substantially Equivalent
Regulation	882.1240

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View the full FDA submission: accessdata.fda.gov

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5.0 IOP & 7.5 IOP PROBES

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