Cleared Traditional

K893641 - COBAS FARA CENTRIFUGAL ANALYZER

K893641 is the FDA 510(k) clearance for COBAS FARA CENTRIFUGAL ANALYZER by Roche Diagnostic Systems, Inc.. It is a Class 1 Chemistry device (product code JJG) cleared through the Traditional 510(k) pathway after a 66-day FDA review.

K893641 · Roche Diagnostic Systems, Inc. · Chemistry device
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Jul 1989
Decision
66d
Days
Class 1
Risk

K893641 is an FDA 510(k) clearance for the COBAS FARA CENTRIFUGAL ANALYZER. Classified as Analyzer, Chemistry, Centrifugal, For Clinical Use (product code JJG), Class I - General Controls.

Submitted by Roche Diagnostic Systems, Inc. (Montclair, US). The FDA issued a Cleared decision on July 20, 1989 after a review of 66 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.2140 - 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 Roche Diagnostic Systems, Inc. devices

Submission Details

510(k) Number K893641 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 15, 1989
Decision Date July 20, 1989
Days to Decision 66 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
22d faster than avg
Panel avg: 88d · This submission: 66d
Pathway characteristics
Predicate-based equivalence.

Device Classification

Product Code JJG Analyzer, Chemistry, Centrifugal, For Clinical Use
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 862.2140
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 - JJG Analyzer, Chemistry, Centrifugal, For Clinical Use

All 16
Devices cleared under the same product code (JJG) and FDA review panel - the closest regulatory comparables to K893641.
COBAS ALPHA
K910222 · Roche Diagnostic Systems, Inc. · Feb 1991
BIOMEK AUTOMATED LABORATORY WORKSTATION W/GENELISA
K903626 · Beckman Instruments, Inc. · Oct 1990
COBAS FARA II CENTRIFUGAL ANALYZER
K893854 · Roche Diagnostic Systems, Inc. · Aug 1989
TECHNICON DAX(TM) SYSTEM
K885203 · Technicon Instruments Corp. · Mar 1989
IL MONARCH 1000 CLINICAL CHEMISTRY ANALYTICAL SYS.
K871973 · Instrumentation Laboratory CO · Jun 1987
BIOMEK 1000C AUTOMATED LABORATORY WORK STATION
K871838 · Beckman Instruments, Inc. · May 1987