K910020 is an FDA 510(k) clearance for the CAPINTEC THYROID UPTAKE SYSTEM-VARIOUS MODELS. Classified as Generator, High-voltage, X-ray, Diagnostic (product code IZO), Class I - General Controls.
Submitted by Capintec Instruments, Inc. (Pittsburgh, US). The FDA issued a Cleared decision on April 8, 1991 after a review of 95 days - within the typical 510(k) review window.
This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1700 - 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.
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