
Landmark Plastics
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TUMBLER, GENERAL MEDICAL MEDI-PAK is an FDA 510(k)-cleared medical device (K760491) manufactured by Landmark Plastics. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 14, 1976. Regulation: 8.

Ansell
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McKesson
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Hollister
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