Oscor, Inc.
GUIDEWIRE, PURSUER SERIES
SKU K130104UPC DQX
In Stock
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IIFDA 510(k) Cleared (K130104)
1
Free shipping on orders over $99 · 30-day returns
Oscor, Inc.
Free shipping on orders over $99 · 30-day returns
GUIDEWIRE, PURSUER SERIES is an FDA 510(k)-cleared medical device (K130104) manufactured by Oscor, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 12, 2013. Regulation: 8.
