Cleared Traditional

K936184 - VIGIL PRX CHEMISTRY CONTROL

K936184 is an FDA 510(k) clearance for VIGIL PRX CHEMISTRY CONTROL, manufactured by Beckman-Diagnostic Systems Group. The device is a Class 1 Toxicology device with product code JJY cleared through the Traditional 510(k) pathway after a 109-day FDA review.

K936184 · Beckman-Diagnostic Systems Group · Toxicology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Apr 1994
Decision
109d
Days
Class 1
Risk

K936184 is an FDA 510(k) clearance for the VIGIL PRX CHEMISTRY CONTROL. Classified as Multi-analyte Controls, All Kinds (assayed) (product code JJY), Class I - General Controls.

Submitted by Beckman-Diagnostic Systems Group (Brea, US). The FDA issued a Cleared decision on April 15, 1994 after a review of 109 days - within the typical 510(k) review window.

This device falls under the Toxicology FDA review panel, regulated under 21 CFR 862.1660 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Toxicology review framework, consistent with the majority of Class II 510(k) submissions.

View all Beckman-Diagnostic Systems Group devices

FDA 510(k) Submission Details - K936184

510(k) Number K936184 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 27, 1993
Decision Date April 15, 1994
Days to Decision 109 days
Submission Type Traditional
Review Panel Toxicology (TX)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
22d slower than avg
Panel avg: 87d · This submission: 109d
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 599
Devices cleared under the same product code (JJY) and FDA review panel - the closest regulatory comparables to K936184.
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