Oscor, Inc.
SAFESEPT TRANSSEPTAL TROCAR GUIDEWIRE
SKU K081986UPC DRC
In Stock
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IIFDA 510(k) Cleared (K081986)
1
Free shipping on orders over $99 · 30-day returns
Oscor, Inc.
Free shipping on orders over $99 · 30-day returns
SAFESEPT TRANSSEPTAL TROCAR GUIDEWIRE is an FDA 510(k)-cleared medical device (K081986) 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 November 13, 2008. Regulation: 8.
