Who is the manufacturer of REVISED LABELING FOR ADX PHENCYCLIDINE?

Abbott Laboratories filed the 510(k) submission for REVISED LABELING FOR ADX PHENCYCLIDINE (K880011).

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

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

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

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

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

K880011 · Abbott Laboratories · LCL · Feb 11, 1988 · TX

Device Facts

Record ID	K880011
Device Name	REVISED LABELING FOR ADX PHENCYCLIDINE
Applicant	Abbott Laboratories
Product Code	LCL · TX
Decision Date	Feb 11, 1988
Decision	SESE
Submission Type	Traditional
Device Class	Class U

REVISED LABELING FOR ADX PHENCYCLIDINE

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