Dau I, Dau II, Dau III and Dau IV Control Urine

FDA 510(k) K893835 · Ciba Corning Diagnostics Corp.

Substantially Equivalent

510(k) numberK893835

Submission

Device name
Dau I, Dau II, Dau III and Dau IV Control Urine
Applicant
Ciba Corning Diagnostics Corp.
East Walpole, MA, US
Received
May 24, 1989
Decision date
July 25, 1989
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DIF – Drug Mixture Control Materials
Device class
Class I (low risk)
Regulation
21 CFR 862.3280
Specialty
Clinical Toxicology

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Questions and answers

When was Dau I, Dau II, Dau III and Dau IV Control Urine cleared by the FDA?

Dau I, Dau II, Dau III and Dau IV Control Urine (K893835) received a 510(k) decision of Substantially Equivalent on July 25, 1989, 62 days after the submission was received.

What is the product code of K893835?

The FDA product code is DIF – Drug Mixture Control Materials, a Class I (low risk) device regulated under 21 CFR 862.3280.