K-number	K770573
Device name	ACTA-SCANNER R 0200FS
Applicant	Pfizer Medical Systems, Inc.
Product code	JAK
Device class	Class II
Decision date	Mar 30, 1977
Decision	Substantially Equivalent
Regulation	892.1750

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View the full FDA submission: accessdata.fda.gov

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ACTA-SCANNER R 0200FS

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