Aca(R) Urine Phencyclidine (U PCP) Screen Method

FDA 510(k) K911725 · E.I. Dupont DE Nemours & Co., Inc.

Substantially Equivalent

510(k) numberK911725

Submission

Device name
Aca(R) Urine Phencyclidine (U PCP) Screen Method
Applicant
E.I. Dupont DE Nemours & Co., Inc.
Wilmington, DE, US
Received
April 17, 1991
Decision date
June 3, 1991
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
LCM – Enzyme Immunoassay, Phencyclidine
Device class
Unclassified

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Questions and answers

When was Aca(R) Urine Phencyclidine (U PCP) Screen Method cleared by the FDA?

Aca(R) Urine Phencyclidine (U PCP) Screen Method (K911725) received a 510(k) decision of Substantially Equivalent on June 3, 1991, 47 days after the submission was received.

What is the product code of K911725?

The FDA product code is LCM – Enzyme Immunoassay, Phencyclidine, a Unclassified device.