Cabot Medical Corp.
3000 ELECTRONIC INSUFFLATOR MODIFICATION
SKU K934115UPC HIF
In Stock
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IIFDA 510(k) Cleared (K934115)
1
Free shipping on orders over $99 · 30-day returns
Cabot Medical Corp.
Free shipping on orders over $99 · 30-day returns
3000 ELECTRONIC INSUFFLATOR MODIFICATION is an FDA 510(k)-cleared medical device (K934115) manufactured by Cabot Medical Corp.. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 14, 1995. Regulation: 8.
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