K900773 is an FDA 510(k) clearance for the NUCLEAR MAX. Classified as Camera, Scintillation (gamma) (product code IYX), Class I - General Controls.
Submitted by Scientific Imaging, Inc. (Littleton, US). The FDA issued a Cleared decision on May 23, 1990 after a review of 96 days - within the typical 510(k) review window.
This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1100 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Radiology review framework, consistent with the majority of Class II 510(k) submissions.
View all Scientific Imaging, Inc. devices