STERIS Corporation
enspire 300 Series Automated Endoscope Reprocessor
SKU K232918UPC NZA
In Stock
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IIFDA 510(k) Cleared (K232918)
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Free shipping on orders over $99 · 30-day returns
STERIS Corporation
Free shipping on orders over $99 · 30-day returns
enspire 300 Series Automated Endoscope Reprocessor is an FDA 510(k)-cleared medical device (K232918) manufactured by STERIS Corporation. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 2, 2023. Regulation: 8.
