Stryker Instruments
MODIFICATION TO STRYKER PAINPUMP2
SKU K030885UPC FRN
In Stock
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IIFDA 510(k) Cleared (K030885)
1
Free shipping on orders over $99 · 30-day returns
Stryker Instruments
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO STRYKER PAINPUMP2 is an FDA 510(k)-cleared medical device (K030885) manufactured by Stryker Instruments. 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 April 17, 2003. Regulation: 8.
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