Cleared Traditional

K871977 - DADE MONI-TROL CHEMISTRY CONTROL/CALIBR...

K871977 is the FDA 510(k) clearance for DADE MONI-TROL CHEMISTRY CONTROL/CALIBR... by American Dade. It is a Class 1 Chemistry device (product code JJY) cleared through the Traditional 510(k) pathway after a 48-day FDA review.

K871977 · American Dade · Chemistry device
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Jul 1987
Decision
48d
Days
Class 1
Risk

K871977 is an FDA 510(k) clearance for the DADE MONI-TROL CHEMISTRY CONTROL/CALIBRATOR. Classified as Multi-analyte Controls, All Kinds (assayed) (product code JJY), Class I - General Controls.

Submitted by American Dade (Santa Ana, US). The FDA issued a Cleared decision on July 9, 1987 after a review of 48 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1660 - the FDA in vitro diagnostics and chemistry 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 American Dade devices

Submission Details

510(k) Number K871977 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 22, 1987
Decision Date July 09, 1987
Days to Decision 48 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
40d faster than avg
Panel avg: 88d · This submission: 48d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code JJY Multi-analyte Controls, All Kinds (assayed)
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 862.1660
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 - JJY Multi-analyte Controls, All Kinds (assayed)

All 463
Devices cleared under the same product code (JJY) and FDA review panel - the closest regulatory comparables to K871977.
PRECINORM L
K874230 · Boehringer Mannheim Corp. · Nov 1987
BIOTROL-33 PLUS PATHOLOGIQUE ASSAYED CHEM. CONTROL
K872777 · Biotrol, USA, Inc. · Aug 1987
BIOTROL-33 PLUS ASSAYED CHEMISTRY CONTROL SERUM
K872785 · Biotrol, USA, Inc. · Aug 1987
LIQUICHEK PEDIATRIC CONTROL LEVELS I AND II
K872227 · Bio-Rad · Jul 1987
QM2/QM300 CONTROL A PACK
K871342 · Kallestad Diag, A Div. of Erbamont, Inc. · May 1987
SERACHEM LIQUID SPINAL FLUID CONTROL (HUMAN)
K871058 · Fisher Scientific Co., LLC · Apr 1987