Cleared Traditional

K894542 - ELSCINT'S EXEL 2400E CT SCANNER

K894542 is the FDA 510(k) clearance for ELSCINT'S EXEL 2400E CT SCANNER by Elscint, Inc.. It is a Class 2 Radiology device (product code JAK) cleared through the Traditional 510(k) pathway after a 49-day FDA review.

K894542 · Elscint, Inc. · Radiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Sep 1989
Decision
49d
Days
Class 2
Risk

K894542 is an FDA 510(k) clearance for the ELSCINT'S EXEL 2400E CT SCANNER. Classified as System, X-ray, Tomography, Computed (product code JAK), Class II - Special Controls.

Submitted by Elscint, Inc. (Hackensack, US). The FDA issued a Cleared decision on September 7, 1989 after a review of 49 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1750 - the FDA radiology and imaging software oversight 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 Elscint, Inc. devices

Submission Details

510(k) Number K894542 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 20, 1989
Decision Date September 07, 1989
Days to Decision 49 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
58d faster than avg
Panel avg: 107d · This submission: 49d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code JAK System, X-ray, Tomography, Computed
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1750
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 Radiology devices follow this clearance model.

Regulatory Peers - JAK System, X-ray, Tomography, Computed

All 608
Devices cleared under the same product code (JAK) and FDA review panel - the closest regulatory comparables to K894542.
TCT-300S - UPGRADE
K900233 · Toshiba America Medical Systems, In.C · Feb 1990
SHIMADZU WHOLE BODY X-RAY CT SCANNER SCT-3000TE
K894888 · Shimadzu Medical Systems · Jan 1990
SHIMADZU WHOLE BODY X-RAY CT SCANNER SCT-3000TF
K894887 · Shimadzu Medical Systems · Dec 1989
CT HILIGHT ADVANTAGE
K894269 · GE Medical Systems · Sep 1989
CT SYTEC 3000
K893820 · General Electric Co. · Aug 1989
TCT-600HQ COMPU TOMO(CT)XRAY/HEAD/WHOLE BODY EXAM
K884555 · Toshiba Medical Systems · Feb 1989