
E.I. Dupont DE Nemours & Co., Inc.
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ACA DU PONT METHOTREXATE (MTHO) METHOD is an FDA 510(k)-cleared medical device (K884744) manufactured by E.I. Dupont DE Nemours & Co., Inc.. This device is classified under the Unknown specialty. FDA Device Class U. FDA clearance granted on January 29, 1989.

Ansell
SKU MSC846624

Princeton BioMeditech Corp.
SKU K014192

McKesson
SKU VM-1270030

Hollister
SKU VM-1270031