Cleared Traditional

K852768 - ORALIX PANORAMIC D.C.

K852768 is the FDA 510(k) clearance for ORALIX PANORAMIC D.C. by Philips Medical Systems, Inc.. It is a Class 2 Radiology device (product code IZF) cleared through the Traditional 510(k) pathway after a 83-day FDA review.

K852768 · Philips Medical Systems, Inc. · Radiology device
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Sep 1985
Decision
83d
Days
Class 2
Risk

K852768 is an FDA 510(k) clearance for the ORALIX PANORAMIC D.C.. Classified as System, X-ray, Tomographic (product code IZF), Class II - Special Controls.

Submitted by Philips Medical Systems, Inc. (5680 Da Best, NL). The FDA issued a Cleared decision on September 19, 1985 after a review of 83 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1740 - 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 Philips Medical Systems, Inc. devices

Submission Details

510(k) Number K852768 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 28, 1985
Decision Date September 19, 1985
Days to Decision 83 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
24d faster than avg
Panel avg: 107d · This submission: 83d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code IZF System, X-ray, Tomographic
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1740
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 - IZF System, X-ray, Tomographic

All 24
Devices cleared under the same product code (IZF) and FDA review panel - the closest regulatory comparables to K852768.
TOMO-LINK
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