K-number	K940037
Device name	I.D. AND SEAKEM GTG AGAROSES
Applicant	Fmc Corp.
Product code	JZR
Device class	Class I
Decision date	Feb 24, 1995
Decision	Substantially Equivalent
Regulation	866.4900

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View the full FDA submission: accessdata.fda.gov

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I.D. AND SEAKEM GTG AGAROSES

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