K870236 is an FDA 510(k) clearance for the PANORAMIC X-RAY MODEL PC-1000. Classified as Unit, X-ray, Extraoral With Timer (product code EHD), Class II - Special Controls.
Submitted by Panoramic Corp. (Fort Wayne, US). The FDA issued a Cleared decision on February 13, 1987 after a review of 23 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.
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