Cleared Traditional

STYROFOAM CUTTERS FOR BLOCK CASTING SYSTEM (K010062) - FDA 510(k) Clearance

Class II Radiology device cleared through predicate-based substantial equivalence - typically does not require clinical trials.

K010062 · Arplay Medical S.A. · Radiology device
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Optimized for regulatory review, auditing and printing
Mar 2001
Decision
64d
Days
Class 2
Risk

K010062 is an FDA 510(k) clearance for the STYROFOAM CUTTERS FOR BLOCK CASTING SYSTEM. Classified as Accelerator, Linear, Medical (product code IYE), Class II - Special Controls.

Submitted by Arplay Medical S.A. (Izeure, Cote D'Or, FR). The FDA issued a Cleared decision on March 13, 2001 after a review of 64 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.5050 - 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 Arplay Medical S.A. devices

Submission Details

510(k) Number K010062 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 08, 2001
Decision Date March 13, 2001
Days to Decision 64 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
43d faster than avg
Panel avg: 107d · This submission: 64d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code IYE Accelerator, Linear, Medical
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.5050
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 - IYE Accelerator, Linear, Medical

All 204
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PORTALVISION
K003636 · Varian Medical Systems, Inc. · Feb 2001
VARIS 1.4G
K001643 · Varian Medical Systems, Inc. · Jun 2000
PRIMUS
K993425 · Siemens Medical Solutions USA, Inc. · Nov 1999