Cleared Traditional

K954247 - SYSCON CONTROL ASSAYED & UNASSAYED

K954247 is an FDA 510(k) clearance for SYSCON CONTROL ASSAYED & UNASSAYED, manufactured by Scantibodies Laboratory, Inc.. The device is a Class 1 Chemistry device with product code JJY cleared through the Traditional 510(k) pathway after a 156-day FDA review.

K954247 · Scantibodies Laboratory, Inc. · Chemistry device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Feb 1996
Decision
156d
Days
Class 1
Risk

K954247 is an FDA 510(k) clearance for the SYSCON CONTROL ASSAYED & UNASSAYED. Classified as Multi-analyte Controls, All Kinds (assayed) (product code JJY), Class I - General Controls.

Submitted by Scantibodies Laboratory, Inc. (Miami, US). The FDA issued a Cleared decision on February 14, 1996 after a review of 156 days - an extended review 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Chemistry review framework, consistent with the majority of Class II 510(k) submissions.

View all Scantibodies Laboratory, Inc. devices

FDA 510(k) Submission Details - K954247

510(k) Number K954247 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 11, 1995
Decision Date February 14, 1996
Days to Decision 156 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
68d slower than avg
Panel avg: 88d · This submission: 156d
Pathway characteristics
Predicate-based equivalence.

JJY Device Classification - Class 1, General Controls

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 545
Devices cleared under the same product code (JJY) and FDA review panel - the closest regulatory comparables to K954247.
LIPID CONTROL
K960862 · Medical Analysis Systems, Inc. · Apr 1996
SYSCON TURMOR MARKER CONTROL
K955812 · Scantibodies Laboratory, Inc. · Mar 1996
N/T PROTEIN CONTROL SY/L, M AND H
K955858 · Behring Diagnostics, Inc. · Feb 1996
NOVA CHEMISTRY LINEARITY SET F, LEVELS 1, 2, 3, AND 4
K955252 · Nova Biomedical Corp. · Feb 1996
NOVA CHEMISTRY PERFORMANCE CHECK SOLUTION
K955260 · Nova Biomedical Corp. · Feb 1996
NOVA CHEMISTRY CONTROLS, LEVELS 1 AND 2
K955264 · Nova Biomedical Corp. · Feb 1996