Cleared Traditional

K862858 - CBC-CAL (TM) PLUS/MULTIPLE

K862858 is the FDA 510(k) clearance for CBC-CAL (TM) PLUS/MULTIPLE by R&D Systems, Inc.. It is a Class 2 Hematology device (product code KRX) cleared through the Traditional 510(k) pathway after a 23-day FDA review.

K862858 · R&D Systems, Inc. · Hematology device
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Aug 1986
Decision
23d
Days
Class 2
Risk

K862858 is an FDA 510(k) clearance for the CBC-CAL (TM) PLUS/MULTIPLE. Classified as Calibrator For Cell Indices (product code KRX), Class II - Special Controls.

Submitted by R&D Systems, Inc. (Minneapolis, US). The FDA issued a Cleared decision on August 21, 1986 after a review of 23 days - a notably fast clearance cycle.

This device falls under the Hematology FDA review panel, regulated under 21 CFR 864.8150 - the FDA hematology 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: 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 R&D Systems, Inc. devices

Submission Details

510(k) Number K862858 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 29, 1986
Decision Date August 21, 1986
Days to Decision 23 days
Submission Type Traditional
Review Panel Hematology (HE)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
90d faster than avg
Panel avg: 113d · This submission: 23d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code KRX Calibrator For Cell Indices
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 864.8150
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 Hematology devices follow this clearance model.

Regulatory Peers - KRX Calibrator For Cell Indices

All 7
Devices cleared under the same product code (KRX) and FDA review panel - the closest regulatory comparables to K862858.
CD-CAL PLUS CALIBRATOR
K003991 · R&D Systems, Inc. · Jan 2001
CBC-CAL PLUS HEMATOLOGY CALIBRATOR
K955925 · R&D Systems, Inc. · Feb 1996
3K-CAL HEMATOLOGY CALIBRATOR/MULTIPLE
K912357 · R&D Systems, Inc. · Jul 1991
DADE HEMATOLOGY CALIBRATOR
K831140 · American Dade · Jun 1983
CELL-CHEX RBC
K811741 · Streck Laboratories, Inc. · Sep 1981