Medtronic, Inc.
Cardioblate Gemini-s 49260 Surgical Ablation Device; Cardioblate Gemini-s 49351 Surgical Ablation Device
SKU K223508UPC OCL
In Stock
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IIFDA 510(k) Cleared (K223508)
1
Free shipping on orders over $99 · 30-day returns
Medtronic, Inc.
Free shipping on orders over $99 · 30-day returns
Cardioblate Gemini-s 49260 Surgical Ablation Device; Cardioblate Gemini-s 49351 Surgical Ablation Device is an FDA 510(k)-cleared medical device (K223508) 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 December 21, 2022. Regulation: 8.
