
Baxter Diagnostics, Inc.
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BARTELS HERPES SIMPLEX VIRUS 1 IGM EIA is an FDA 510(k)-cleared medical device (K922334) manufactured by Baxter Diagnostics, Inc.. This device is classified under the Microbiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 14, 1992. Regulation: 8.

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