K-number	K910178
Device name	ACTH IRMA KIT MITSUBISHI YUKA
Applicant	Science Regulatory Services Intl.
Product code	CKG
Device class	Class II
Decision date	May 22, 1991
Decision	Substantially Equivalent
Regulation	862.1025

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View the full FDA submission: accessdata.fda.gov

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ACTH IRMA KIT MITSUBISHI YUKA

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