Who is the manufacturer of REVISED LABELING FOR TDX PHENCYCLIDINE?

Abbott Laboratories filed the 510(k) submission for REVISED LABELING FOR TDX PHENCYCLIDINE (K874484).

What is the FDA product code for REVISED LABELING FOR TDX PHENCYCLIDINE?

LCL. as a Class U device in the TX panel.

What is the regulatory pathway for REVISED LABELING FOR TDX PHENCYCLIDINE?

510(k) clearance (submission type: Traditional).

Who can help prepare an FDA 510(k) submission like REVISED LABELING FOR TDX PHENCYCLIDINE?

Innolitics — a medical-device software consultancy — provides regulatory and engineering support for FDA 510(k) submissions. See https://innolitics.com/services/510ks/ or contact https://innolitics.com/contact.

REVISED LABELING FOR TDX PHENCYCLIDINE

K874484 · Abbott Laboratories · LCL · Nov 23, 1987 · TX

Device Facts

Record ID	K874484
Device Name	REVISED LABELING FOR TDX PHENCYCLIDINE
Applicant	Abbott Laboratories
Product Code	LCL · TX
Decision Date	Nov 23, 1987
Decision	SESE
Submission Type	Traditional
Device Class	Class U

REVISED LABELING FOR TDX PHENCYCLIDINE

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