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U.S. Department of Health and Human Services

510(k) Premarket Notification
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1 to 6 of 6 Results
ProductCode: OCL Applicant: MEDTRONIC INC. Decision Date To: 05/29/2024
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cardioblate gemini-s 49260 surgical ablation device; cardioblate gemini-s 49351 surgical ablation device Medtronic Inc. K223508 12/22/2022
cardioblate cryoflex surgical ablation system MEDTRONIC INC. K123733 04/01/2013
cardioblate cryoflex surgical ablation probes MEDTRONIC INC. K121878 11/02/2012
cardioblate gemini surgical ablation device MEDTRONIC INC. K121767 07/13/2012
cardioblate maps surgical mapping, ablation, pacing , and sensing device MEDTRONIC INC. K121451 06/14/2012
cardioblate 68000 gnerator, bp2 surgical ablation device, lp surgical ablation device, gemini-ssurgical ablation device MEDTRONIC INC. K080509 05/05/2008
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