K-number	K802308
Device name	T/K (ATA/AMA) UNIVERSAL BIOPAK
Applicant	Bioware Products
Product code	DBM
Device class	Class II
Decision date	Dec 1, 1980
Decision	Substantially Equivalent
Regulation	866.5090

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View the full FDA submission: accessdata.fda.gov

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T/K (ATA/AMA) UNIVERSAL BIOPAK

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