Cleared Traditional

K880373 - IONOMETER E-HK AND ACCESSORIES

K880373 is the FDA 510(k) clearance for IONOMETER E-HK AND ACCESSORIES by Smash Ent., Inc.. It is a Class 2 Hematology device (product code GKF) cleared through the Traditional 510(k) pathway after a 50-day FDA review.

K880373 · Smash Ent., Inc. · Hematology device
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Mar 1988
Decision
50d
Days
Class 2
Risk

K880373 is an FDA 510(k) clearance for the IONOMETER E-HK AND ACCESSORIES. Classified as Instrument, Hematocrit, Automated (product code GKF), Class II - Special Controls.

Submitted by Smash Ent., Inc. (Arden Hills, US). The FDA issued a Cleared decision on March 17, 1988 after a review of 50 days - a notably fast clearance cycle.

This device falls under the Hematology FDA review panel, regulated under 21 CFR 864.5600 - 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 Smash Ent., Inc. devices

Submission Details

510(k) Number K880373 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 27, 1988
Decision Date March 17, 1988
Days to Decision 50 days
Submission Type Traditional
Review Panel Hematology (HE)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
63d faster than avg
Panel avg: 113d · This submission: 50d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code GKF Instrument, Hematocrit, Automated
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 864.5600
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 - GKF Instrument, Hematocrit, Automated

All 10
Devices cleared under the same product code (GKF) and FDA review panel - the closest regulatory comparables to K880373.
MARATHON 6K GENERAL-PURPOSE CENTRIFUGE
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MARATHON 13K/H MICROHEMATOCRIT CENTRIFUGE
K915441 · Fisher Scientific Co., LLC · Jan 1992
NEW COBE SATURATION/HEMATOCRIT MONITOR
K904336 · Cobe Laboratories, Inc. · Dec 1990
SORVALL CAPSPIN MICROHEMATOCRIT CENTRIFUGE
K864646 · E.I. Dupont DE Nemours & Co., Inc. · Jan 1987
STAT-CRIT HEMATOCRIT MEASURING INSTRU
K802199 · United States Surgical, A Division of Tyco Healthc · Feb 1981
CUTTER/COMPUR MINI CENTRIFUGE
K781059 · Cutter Laboratories, Inc. · Aug 1978