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FDA grants 510(k) clearance for Huntleigh’s CTG Analysis
The FDA has granted 510(k) approval for UK-based Huntleigh Healthcare’s Dawes-Redman CTG Analysis for foetal monitoring applications. The post FDA grants 510(k) clearance for Huntleigh’s CTG Analysis appeared first on Medical Device Network.
The FDA has granted 510(k) approval for UK-based Huntleigh Healthcare’s Dawes-Redman CTG Analysis for foetal monitoring applications.
The post FDA grants 510(k) clearance for Huntleigh’s CTG Analysis appeared first on Medical Device Network.
