
Steris Corporations
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Celerity HP Chemical Indicator (CI) is an FDA 510(k)-cleared medical device (K183295) manufactured by Steris Corporations. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 3, 2019. Regulation: 8.

Ansell
SKU MSC846624

Princeton BioMeditech Corp.
SKU K014192

McKesson
SKU VM-1270030

Hollister
SKU VM-1270031