Cleared Traditional

K926131 - OPUS MAGNUM ANALYZER

K926131 is the FDA 510(k) clearance for OPUS MAGNUM ANALYZER by Pb Diagnostic Systems, Inc.. It is a Class 1 Chemistry device (product code KHO) cleared through the Traditional 510(k) pathway after a 182-day FDA review.

K926131 · Pb Diagnostic Systems, Inc. · Chemistry device
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Jun 1993
Decision
182d
Days
Class 1
Risk

K926131 is an FDA 510(k) clearance for the OPUS MAGNUM ANALYZER. Classified as Fluorometer, For Clinical Use (product code KHO), Class I - General Controls.

Submitted by Pb Diagnostic Systems, Inc. (Westwood, US). The FDA issued a Cleared decision on June 7, 1993 after a review of 182 days - an extended review cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.2560 - 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 Pb Diagnostic Systems, Inc. devices

Submission Details

510(k) Number K926131 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 07, 1992
Decision Date June 07, 1993
Days to Decision 182 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
94d slower than avg
Panel avg: 88d · This submission: 182d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code KHO Fluorometer, For Clinical Use
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 862.2560
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 - KHO Fluorometer, For Clinical Use

All 24
Devices cleared under the same product code (KHO) and FDA review panel - the closest regulatory comparables to K926131.
TRIAGE STATMETER
K973547 · Biosite Incorporated · Jan 1998
AIA NEXIA-AUTOMATED ENZYME IMMUNOASSAY SYSTEM
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FLUOROSCAN NEONATAL
K950415 · Isolab, Inc. · Sep 1995
MICROLITE MICROTITER PLATE LUMINOMETER ML2200
K920888 · Dynatech Laboratories, Inc. · Mar 1992
STRATUS IINTELLECT IMMUNOASSAY SYSTEM
K913130 · Baxter Healthcare Corp · Sep 1991
DELFIA PLATE FLUOROMETER 1232
K895240 · Pharmacia, Inc. · Oct 1989