Cleared Traditional

K871486 - (FPIA) ASSAY BUFFER

K871486 is the FDA 510(k) clearance for (FPIA) ASSAY BUFFER by Windsor Laboratories, Inc.. It is a Class 1 Chemistry device (product code JJF) cleared through the Traditional 510(k) pathway after a 23-day FDA review.

K871486 · Windsor Laboratories, Inc. · Chemistry device
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May 1987
Decision
23d
Days
Class 1
Risk

K871486 is an FDA 510(k) clearance for the (FPIA) ASSAY BUFFER. Classified as Analyzer, Chemistry, Micro, For Clinical Use (product code JJF), Class I - General Controls.

Submitted by Windsor Laboratories, Inc. (Garland, US). The FDA issued a Cleared decision on May 8, 1987 after a review of 23 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.2170 - 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 Windsor Laboratories, Inc. devices

Submission Details

510(k) Number K871486 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 15, 1987
Decision Date May 08, 1987
Days to Decision 23 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
65d faster than avg
Panel avg: 88d · This submission: 23d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code JJF Analyzer, Chemistry, Micro, For Clinical Use
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 862.2170
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 - JJF Analyzer, Chemistry, Micro, For Clinical Use

All 35
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