
Bailey Mfg. Co.
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PRO. HI-LOW TREATMENT TABLES MODELS 4050,4070,4090 is an FDA 510(k)-cleared medical device (K932237) manufactured by Bailey Mfg. Co.. This device is classified under the Physical Medicine specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on July 21, 1993. 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