Cleared Traditional

K043612 - ORTHOPANTOMOGRAPH OP200, OP200D, AND ORTHOCEPH OC200, OC200D

K043612 is an FDA 510(k) clearance for ORTHOPANTOMOGRAPH OP200, manufactured by Instrumentarium Corp. Imaging Division. The device is a Class 2 Radiology device with product code EHD cleared through the Traditional 510(k) pathway after a 41-day FDA review.

K043612 · Instrumentarium Corp. Imaging Division · Radiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Feb 2005
Decision
41d
Days
Class 2
Risk

K043612 is an FDA 510(k) clearance for the ORTHOPANTOMOGRAPH OP200, OP200D, AND ORTHOCEPH OC200, OC200D. Classified as Unit, X-ray, Extraoral With Timer (product code EHD), Class II - Special Controls.

Submitted by Instrumentarium Corp. Imaging Division (Milwaukee, US). The FDA issued a Cleared decision on February 9, 2005 after a review of 41 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 872.1800 - 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 Instrumentarium Corp. Imaging Division devices

FDA 510(k) Submission Details - K043612

510(k) Number K043612 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 30, 2004
Decision Date February 09, 2005
Days to Decision 41 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
66d faster than avg
Panel avg: 107d · This submission: 41d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

EHD Device Classification - Class 2, Special Controls

Product Code EHD Unit, X-ray, Extraoral With Timer
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.1800
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 - EHD Unit, X-ray, Extraoral With Timer

All 120
Devices cleared under the same product code (EHD) and FDA review panel - the closest regulatory comparables to K043612.
HELIODENT PLUS
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IN EXAM INTRAORAL DENTAL X-RAY SYSTEM
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TROPHYPAN C WITH ORTHOIMAGING/OMSIMAGING ACCESSORY
K040556 · Eastman Kodak Company · Apr 2004
TROPHYPAN AND TROPHYPAN C
K033690 · Trophy Radiologie · Feb 2004