Hycor Sentry Drugs of Abuse Urine Control:

FDA 510(k) K890957 · Hycor Biomedical, Inc.

Substantially Equivalent

510(k) numberK890957

Submission

Device name
Hycor Sentry Drugs of Abuse Urine Control:
Applicant
Hycor Biomedical, Inc.
Garden Grove, CA, US
Received
February 27, 1989
Decision date
March 9, 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 Hycor Sentry Drugs of Abuse Urine Control: cleared by the FDA?

Hycor Sentry Drugs of Abuse Urine Control: (K890957) received a 510(k) decision of Substantially Equivalent on March 9, 1989, 10 days after the submission was received.

What is the product code of K890957?

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