
Medtronic Minimed
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POLYFIN QR SUBCUTANEOUS INFUSION SET is an FDA 510(k)-cleared medical device (K954969) manufactured by Medtronic Minimed. 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 February 21, 1996. Regulation: 8.

Ansell
SKU MSC846624

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SKU K014192

McKesson
SKU VM-1270030

Hollister
SKU VM-1270031