Cleared Traditional

K843110 - ROCHE STANDARDS FOR CHOLESTEROL

K843110 is the FDA 510(k) clearance for ROCHE STANDARDS FOR CHOLESTEROL by Roche Diagnostic Systems, Inc.. It is a Class 2 Chemistry device (product code JIS) cleared through the Traditional 510(k) pathway after a 28-day FDA review.

K843110 · Roche Diagnostic Systems, Inc. · Chemistry device
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Sep 1984
Decision
28d
Days
Class 2
Risk

K843110 is an FDA 510(k) clearance for the ROCHE STANDARDS FOR CHOLESTEROL. Classified as Calibrator, Primary (product code JIS), Class II - Special Controls.

Submitted by Roche Diagnostic Systems, Inc. (Mchenry, US). The FDA issued a Cleared decision on September 4, 1984 after a review of 28 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 K843110 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 07, 1984
Decision Date September 04, 1984
Days to Decision 28 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
60d faster than avg
Panel avg: 88d · This submission: 28d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code JIS Calibrator, Primary
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 - JIS Calibrator, Primary

All 87
Devices cleared under the same product code (JIS) and FDA review panel - the closest regulatory comparables to K843110.
SERALYZER TOTAL BILIRUBIN CALIBRATORS
K855040 · Miles Laboratories, Inc. · Jan 1986
TOTAL BILIRUBIN STANDARDS
K852068 · Data Medical Associates, Inc. · May 1985
80 MG/DL GLUCOSE CONTROL
K844581 · Boehringer Mannheim Corp. · Dec 1984
HICHEM ION 2/4 SERUM RANGE CALIBRATOR
K842449 · Hi Chem, Inc. · Aug 1984
HICHEM ION 2/4 URINE RANGE CALIBRATOR
K842450 · Hi Chem, Inc. · Aug 1984
DUPONT ACA MAGNESIUM CALIBRATOR
K841955 · E.I. Dupont DE Nemours & Co., Inc. · Jun 1984