K200577 is an FDA 510(k) clearance for the RAS 12 Rack, RAS 12 Long Rack, RAS Cycle of the AMSCO 7052HP/7053HP Single Ch.... Classified as Washer, Cleaner, Automated, Endoscope (product code NVE), Class II - Special Controls.
Submitted by STERIS Corporation (Mentor, US). The FDA issued a Cleared decision on April 3, 2020 after a review of 29 days - a notably fast clearance cycle.
This device falls under the General Hospital FDA review panel, regulated under 21 CFR 876.1500 - the FDA general hospital device framework. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.
Device pattern: Iterative device modification. Low regulatory complexity profile. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.
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