Cleared Traditional

K802672 - CARDIOACTIVE DRUGS CONTROL

K802672 is the FDA 510(k) clearance for CARDIOACTIVE DRUGS CONTROL by Fisher Scientific Co., LLC. It is a Class 1 Toxicology device (product code DIF) cleared through the Traditional 510(k) pathway after a 28-day FDA review.

K802672 · Fisher Scientific Co., LLC · Toxicology device
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Nov 1980
Decision
28d
Days
Class 1
Risk

K802672 is an FDA 510(k) clearance for the CARDIOACTIVE DRUGS CONTROL. Classified as Drug Mixture Control Materials (product code DIF), Class I - General Controls.

Submitted by Fisher Scientific Co., LLC (Mchenry, US). The FDA issued a Cleared decision on November 24, 1980 after a review of 28 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 Fisher Scientific Co., LLC devices

Submission Details

510(k) Number K802672 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 27, 1980
Decision Date November 24, 1980
Days to Decision 28 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
59d faster than avg
Panel avg: 87d · This submission: 28d
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 146
Devices cleared under the same product code (DIF) and FDA review panel - the closest regulatory comparables to K802672.
PROFILE ANTI-CONVUL. SET ASSAYED S. CTL.
K803039 · General Diagnostics · Dec 1980
DIGOXIN & PHENYTOIN CONTROL SERA
K803097 · Amersham Corp. · Dec 1980
BECKMAN ICS DRUG CONTROL SERA
K802854 · Beckman Instruments, Inc. · Dec 1980
THERA CHEM
K782128 · Fisher Scientific Co., LLC · Mar 1979
SERUM, CONTROL, DRUGS, ANTIARRYTHMIC
K780960 · Vitek Systems, Inc. · Dec 1978