K-number	K874484
Device name	REVISED LABELING FOR TDX PHENCYCLIDINE
Applicant	Abbott Laboratories
Product code	LCL
Device class	Class U
Decision date	Nov 23, 1987
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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REVISED LABELING FOR TDX PHENCYCLIDINE

Everything you need for a 510(k) submission. Nothing you don't.