Cleared Traditional

K023636 - BLOCKING TRAY

K023636 is an FDA 510(k) clearance for BLOCKING TRAY, manufactured by Southeastern Radiation Products, Inc.. The device is a Class 2 Radiology device with product code IYE cleared through the Traditional 510(k) pathway after a 23-day FDA review.

K023636 · Southeastern Radiation Products, Inc. · Radiology device
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Nov 2002
Decision
23d
Days
Class 2
Risk

K023636 is an FDA 510(k) clearance for the BLOCKING TRAY. Classified as Accelerator, Linear, Medical (product code IYE), Class II - Special Controls.

Submitted by Southeastern Radiation Products, Inc. (Sanford, US). The FDA issued a Cleared decision on November 22, 2002 after a review of 23 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.

FDA 510(k) Submission Details - K023636

510(k) Number K023636 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 30, 2002
Decision Date November 22, 2002
Days to Decision 23 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
84d faster than avg
Panel avg: 107d · This submission: 23d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

IYE Device Classification - Class 2, Special Controls

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 724
Devices cleared under the same product code (IYE) and FDA review panel - the closest regulatory comparables to K023636.
NON-INVASIVE PATIENT FIXATION SYSTEM
K023449 · Stryker Leibinger · Jan 2003
ACCULEAF
K021338 · Direx Systems Corp. · Jan 2003
MED-TEC BELLYBOARD, MODELS MT-BBA-01 & MT-BBA-02
K023293 · Med-Tec,Inc. · Dec 2002
KLARITY
K022708 · Larson Products, Inc. · Nov 2002
RADIOSYSTEM/NT, MODEL 80-13020
K020320 · Styker Instruments · Aug 2002
CRANIAL STEREOTACTIC EQUIPMENT
K010065 · Arplay Medical S.A. · Jul 2002
K023636 · BLOCKING TRAY
Download PDF FDA Summary Southeastern Radiatio…