Medtronic, Inc.
CARDIOBLATE 68000 GNERATOR, BP2 SURGICAL ABLATION DEVICE, LP SURGICAL ABLATION DEVICE, GEMINI-SSURGICAL ABLATION DEVICE
SKU K080509UPC OCL
In Stock
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IIFDA 510(k) Cleared (K080509)
1
Free shipping on orders over $99 · 30-day returns
Medtronic, Inc.
Free shipping on orders over $99 · 30-day returns
CARDIOBLATE 68000 GNERATOR, BP2 SURGICAL ABLATION DEVICE, LP SURGICAL ABLATION DEVICE, GEMINI-SSURGICAL ABLATION DEVICE is an FDA 510(k)-cleared medical device (K080509) manufactured by Medtronic, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 4, 2008. Regulation: 8.
