Biotronik, Inc.
MODIFICATION TO BIOTRONIK'S STERILIZATION PROCESS
SKU K023803UPC DTB
In Stock
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IIIFDA 510(k) Cleared (K023803)
1
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Biotronik, Inc.
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO BIOTRONIK'S STERILIZATION PROCESS is an FDA 510(k)-cleared medical device (K023803) manufactured by Biotronik, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on December 10, 2002. Regulation: 8.
