Reverse Medical Corporation
REVERSE MEDICAL REPORT GUIDE CATHETER SYSTEM
SKU K102418UPC DQY
In Stock
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IIFDA 510(k) Cleared (K102418)
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Free shipping on orders over $99 · 30-day returns
Reverse Medical Corporation
Free shipping on orders over $99 · 30-day returns
REVERSE MEDICAL REPORT GUIDE CATHETER SYSTEM is an FDA 510(k)-cleared medical device (K102418) manufactured by Reverse Medical Corporation. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 14, 2011. Regulation: 8.
