K-number	K905115
Device name	BIOVISION ENDOCULAR PROBE
Applicant	Douglas James Donaldson Compliance Services
Product code	HGF
Device class	Class II
Decision date	Feb 11, 1991
Decision	Substantially Equivalent
Regulation	884.5070

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View the full FDA submission: accessdata.fda.gov

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BIOVISION ENDOCULAR PROBE

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