Cleared Traditional

K843112 - ROCHE STANDARDS FOR URIC ACID

K843112 is the FDA 510(k) clearance for ROCHE STANDARDS FOR URIC ACID by Roche Diagnostic Systems, Inc.. It is a Class 2 Chemistry device (product code JIT) cleared through the Traditional 510(k) pathway after a 37-day FDA review.

K843112 · Roche Diagnostic Systems, Inc. · Chemistry device
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Sep 1984
Decision
37d
Days
Class 2
Risk

K843112 is an FDA 510(k) clearance for the ROCHE STANDARDS FOR URIC ACID. Classified as Calibrator, Secondary (product code JIT), Class II - Special Controls.

Submitted by Roche Diagnostic Systems, Inc. (Mchenry, US). The FDA issued a Cleared decision on September 13, 1984 after a review of 37 days - a notably fast clearance cycle.

This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1150 - 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 K843112 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 07, 1984
Decision Date September 13, 1984
Days to Decision 37 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
51d faster than avg
Panel avg: 88d · This submission: 37d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code JIT Calibrator, Secondary
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 862.1150
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Chemistry devices follow this clearance model.

Regulatory Peers - JIT Calibrator, Secondary

All 150
Devices cleared under the same product code (JIT) and FDA review panel - the closest regulatory comparables to K843112.
DIRECT BILIRUBEN CALIBRATIONS
K852067 · Data Medical Associates, Inc. · May 1985
CHEM TRAK TRI-POINT LIQUID BILIRUBIN CALIBRATOR,I/
K851670 · Medical Analysis Systems, Inc. · May 1985
TRIGLYCERIDE CALIBRATOR
K844468 · Sigma Diagnostics, Inc. · Dec 1984
ACTH STANDARD MATRIX
K842099 · Diagnostic Systems Laboratories, Inc. · Aug 1984
ALCOHOL & AMMONIA CALIBRATOR I
K840771 · American Dade · Apr 1984
ALCOHOL & AMMONIA CALIBRATOR II
K840772 · American Dade · Apr 1984