
Baxter Healthcare Corporation
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Solution Set with 1.2 Micron Air Eliminating Filter is an FDA 510(k)-cleared medical device (K161808) manufactured by Baxter Healthcare Corporation. 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 June 20, 2017. Regulation: 8.

Ansell
SKU MSC846624

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McKesson
SKU VM-1270030

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SKU VM-1270031