Cleared Traditional

K890957 - HYCOR SENTRY DRUGS OF ABUSE URINE CONTROL:

K890957 is the FDA 510(k) clearance for HYCOR SENTRY DRUGS OF ABUSE URINE CONTROL: by Hycor Biomedical, Inc.. It is a Class 1 Toxicology device (product code DIF) cleared through the Traditional 510(k) pathway after a 10-day FDA review.

K890957 · Hycor Biomedical, Inc. · Toxicology device
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Mar 1989
Decision
10d
Days
Class 1
Risk

K890957 is an FDA 510(k) clearance for the HYCOR SENTRY DRUGS OF ABUSE URINE CONTROL:. Classified as Drug Mixture Control Materials (product code DIF), Class I - General Controls.

Submitted by Hycor Biomedical, Inc. (Garden Grove, US). The FDA issued a Cleared decision on March 9, 1989 after a review of 10 days - a notably fast clearance cycle.

This device falls under the Toxicology FDA review panel, regulated under 21 CFR 862.3280 - the FDA toxicology device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Hycor Biomedical, Inc. devices

Submission Details

510(k) Number K890957 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 27, 1989
Decision Date March 09, 1989
Days to Decision 10 days
Submission Type Traditional
Review Panel Toxicology (TX)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
77d faster than avg
Panel avg: 87d · This submission: 10d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code DIF Drug Mixture Control Materials
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 862.3280
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - DIF Drug Mixture Control Materials

All 143
Devices cleared under the same product code (DIF) and FDA review panel - the closest regulatory comparables to K890957.
BIO-RAD BLIND PERFOR. SPECIMEN SET FOR NIDA REG.
K895816 · Bio-Rad · Dec 1989
KIT- CIBA CORNING L-TDM I, II, III
K893682 · Ciba Corning Diagnostics Corp. · Sep 1989
DAU I, DAU II, DAU III AND DAU IV CONTROL URINE
K893835 · Ciba Corning Diagnostics Corp. · Jul 1989
EMIT (R) HVA NEGATIVE URINE
K883210 · Syva Co. · Sep 1988
DADE TDM CONTROL
K883190 · Baxter Healthcare Corp · Sep 1988
EMIT HVA CONTROL KIT
K881944 · Syva Co. · Jul 1988