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Sentreheart, Inc.

5 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
LARIAT RS Suture Delivery Device (K153096)Sentreheart, Inc.2015-11-25
LARIAT sulture Delivery Device (K142241)Sentreheart, Inc.2014-09-12
LARIAT II SUTURE DELIVERY DEVICE (K090385)Sentreheart, Inc.2009-05-06
FINDRWIRZ GUIDE WIRE SYSTEM (K080364)Sentreheart, Inc.2008-08-11
OCCLUSION BALLOON CATHETER (K070126)Sentreheart, Inc.2008-02-08

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