K-number	K781668
Device name	GAMMA RADIATION STERILIZATION PRECEDURE
Applicant	Cutter Laboratories, Inc.
Product code	KYJ
Device class	Class II
Decision date	Nov 3, 1978
Decision	Substantially Equivalent
Regulation	888.3230

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View the full FDA submission: accessdata.fda.gov

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GAMMA RADIATION STERILIZATION PRECEDURE

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