FDA 510(k)

REVISED LABELING FOR ADX PHENCYCLIDINE

K-Number: K880011 · 1988-02-11

Decision Date1988-02-11

Product CodeLCL

DecisionSubstantially Equivalent

Device Summary

REVISED LABELING FOR ADX PHENCYCLIDINE is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1988-02-11 under 510(k) number K880011. The device is classified under product code LCL. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REVISED LABELING FOR ADX PHENCYCLIDINE?

REVISED LABELING FOR ADX PHENCYCLIDINE is a medical device that received FDA 510(k) clearance on 1988-02-11. The listed applicant is Abbott Laboratories. The 510(k) number is K880011.

When did REVISED LABELING FOR ADX PHENCYCLIDINE receive FDA 510(k) clearance?

REVISED LABELING FOR ADX PHENCYCLIDINE received FDA 510(k) clearance on 1988-02-11, under 510(k) number K880011.

Who is the listed applicant for REVISED LABELING FOR ADX PHENCYCLIDINE?

The FDA 510(k) record lists Abbott Laboratories as the applicant. This does not by itself establish the device manufacturer.

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

The FDA product code for REVISED LABELING FOR ADX PHENCYCLIDINE is LCL.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.