
U.S. Mfg. & Management, Inc.
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MODIFIED I.V. START, RE-START, PEDI AND GERI-KIT is an FDA 510(k)-cleared medical device (K862335) manufactured by U.S. Mfg. & Management, Inc.. This device is classified under the Unknown specialty. FDA clearance granted on July 23, 1986.

Ansell
SKU MSC846624

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SKU VM-1270030

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SKU VM-1270031