K772148 is an FDA 510(k) clearance for the CATHETER, FEMORAL VEIN, SF 6. Classified as Intracatheter, Dialysis (product code FJT), Class II - Special Controls.
Submitted by Sorensen Research (Mchenry, US). The FDA issued a Cleared decision on November 29, 1977 after a review of 15 days - a notably fast clearance cycle.
This device falls under the Hematology FDA review panel, regulated under 21 CFR 876.5820 - the FDA hematology 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: 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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