![WESTMED, INC.'S BLOCKAIDE FILTER [21 CFR 807.87(A)] — view 1](/_next/image?url=https%3A%2F%2Fpixabay.com%2Fget%2Fg9d1ceed6c74c1fbc3c72ecb0ab54f57e612090050c98d7af50009d86faafaca826a9dbcc11c2039db8056c9eaed5e5b1494ed06a1810bc97e009a6bc63a7b6f9_1280.jpg&w=3840&q=75)
Westmed, Inc.
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WESTMED, INC.'S BLOCKAIDE FILTER [21 CFR 807.87(A)] is an FDA 510(k)-cleared medical device (K121382) manufactured by Westmed, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 5, 2012. Regulation: 8.