K-number	K894127
Device name	LUMISCOPE MODEL 1000/APCC MODEL 1000
Applicant	Lumiscope Co., Inc.
Product code	GZJ
Device class	Class II
Decision date	Sep 6, 1989
Decision	Substantially Equivalent
Regulation	882.5890

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View the full FDA submission: accessdata.fda.gov

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LUMISCOPE MODEL 1000/APCC MODEL 1000

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