
Diatech, Inc.
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DIA-H 1/2/3 & DIA-HT 1/2/3 is an FDA 510(k)-cleared medical device (K840801) manufactured by Diatech, Inc.. This device is classified under the Unknown specialty. FDA clearance granted on April 24, 1984.

Ansell
SKU MSC846624

Princeton BioMeditech Corp.
SKU K014192

McKesson
SKU VM-1270030

Hollister
SKU VM-1270031