
Omron Healthcare, Inc.
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OMBRON TWIN-HEAD MASSAGER MODEL HM-101 is an FDA 510(k)-cleared medical device (K935462) manufactured by Omron Healthcare, Inc.. This device is classified under the Physical Medicine specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on March 3, 1994. Regulation: 8.

Synthes (Usa)
SKU K100676
BackorderedMedline
SKU VM-1270020

Cardinal Health
SKU VM-1270026
BackorderedMoog
SKU VM-1270057