
Diatek, Inc.
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DIATEK 600 THERMOMETER SYSTEM is an FDA 510(k)-cleared medical device (K833568) manufactured by Diatek, Inc.. 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 January 9, 1984. Regulation: 8.

Ansell
SKU MSC846624

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McKesson
SKU VM-1270030

Hollister
SKU VM-1270031