K-number	K861966
Device name	MODIFIED IDEIA CHLAMYDIA TEST
Applicant	Boots-Celltech Diagnostics, Inc.
Product code	LJC
Device class	Class I
Decision date	Aug 19, 1986
Decision	Substantially Equivalent
Regulation	866.3120

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View the full FDA submission: accessdata.fda.gov

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MODIFIED IDEIA CHLAMYDIA TEST

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