K863298 is an FDA 510(k) clearance for the DIAMOND MEDICAL, INC., MODEL DM 700. Classified as Electrode, Ph, Stomach (product code FFT), Class I - General Controls.
Submitted by Diamond Medical, Inc. (Saint Paul, US). The FDA issued a Cleared decision on March 17, 1987 after a review of 204 days - an extended review cycle.
This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.1400 - the FDA gastroenterology and urology device 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 Gastroenterology & Urology review framework, consistent with the majority of Class II 510(k) submissions.
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