Cleared Traditional

K863849 - LIQUI-SERA COMBO LIGAND/TDM CONTROLS

K863849 is the FDA 510(k) clearance for LIQUI-SERA COMBO LIGAND/TDM CONTROLS by Biodiagnostic Intl. It is a Class 1 Chemistry device (product code JJY) cleared through the Traditional 510(k) pathway after a 55-day FDA review.

K863849 · Biodiagnostic Intl · Chemistry device
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Nov 1986
Decision
55d
Days
Class 1
Risk

K863849 is an FDA 510(k) clearance for the LIQUI-SERA COMBO LIGAND/TDM CONTROLS. Classified as Multi-analyte Controls, All Kinds (assayed) (product code JJY), Class I - General Controls.

Submitted by Biodiagnostic Intl (La Habra, US). The FDA issued a Cleared decision on November 24, 1986 after a review of 55 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 Biodiagnostic Intl devices

Submission Details

510(k) Number K863849 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 30, 1986
Decision Date November 24, 1986
Days to Decision 55 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
33d faster than avg
Panel avg: 88d · This submission: 55d
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 469
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