REVISED LABELING FOR ADX PHENCYCLIDINE— 510(k) K880011

Name: FDA 510(k) clearance K880011
Creator: U.S. Food and Drug Administration
Published: 1988-02-11

Substantially Equivalent

Abbott Laboratories

FDA 510(k) clearance K880011 for REVISED LABELING FOR ADX PHENCYCLIDINE, Substantially Equivalent on 1988-02-11. Applicant: Abbott Laboratories. Device class: Unclassified.

Clearance details

Applicant: Abbott Laboratories
Product code: Code LCL
Device class: Unclassified
Advisory panel: Unknown
Date received: 1988-01-04
Decision date: 1988-02-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Abbott Park, IL, US

Download summary PDF View on FDA.gov ↗

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