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Intervalve, Inc.

5 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
V8 Balloon Aortic Valvuloplasty Catheter (K152150)Intervalve, Inc.2015-12-18
V8 Transluminal BAV Catheter (K150343)Intervalve, Inc.2015-04-03
V8 TRANSLUMINAL BAV CATHETER (K133607)Intervalve, Inc.2014-02-11
V8 TRANSLUMINAL BAV CATHETER (K132728)Intervalve, Inc.2013-11-22
V8 TRANSLUMINAL BAV CATHETER (K123111)Intervalve, Inc.2013-01-31

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Every clearance here is in the API, with alerts when new ones post.