
General Physiotherapy, Inc.
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PORTA-PULS MUSCLE STIMULATOR is an FDA 510(k)-cleared medical device (K810244) manufactured by General Physiotherapy, Inc.. This device is classified under the Physical Medicine specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on February 25, 1981. Regulation: 8.

Synthes (Usa)
SKU K100676
BackorderedMedline
SKU VM-1270020

Cardinal Health
SKU VM-1270026
BackorderedMoog
SKU VM-1270057