K-number	K821108
Device name	BI PLATE-XLD/HEKTOEN #30012
Applicant	Biomedia, Inc.
Product code	JSI
Device class	Class I
Decision date	May 13, 1982
Decision	Substantially Equivalent
Regulation	866.2360

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View the full FDA submission: accessdata.fda.gov

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BI PLATE-XLD/HEKTOEN #30012

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