
Somatron Co.
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SOMATRON is an FDA 510(k)-cleared medical device (K831394) manufactured by Somatron Co.. This device is classified under the Physical Medicine specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 7, 1983. Regulation: 8.

Synthes (Usa)
SKU K100676
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SKU VM-1270020

Cardinal Health
SKU VM-1270026
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SKU VM-1270057