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Flowcardia, Inc.

11 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
THE CROSSER S6 CATHETER, THE CROSSER SYSTEM ELECTRONICS, MODEL CRUS6, GEN200 (K092175)Flowcardia, Inc.2010-02-17
FLOWCARDIA FLOWMATER INJECTOR, MODEL INJ 100 (K090621)Flowcardia, Inc.2009-06-19
THE CROSSER 14 OTW CATHETER, MODEL CRU014 (K091254)Flowcardia, Inc.2009-05-29
MODIFICATION TO THE CROSSER SYSTEM (K091119)Flowcardia, Inc.2009-05-15
MICROSHEATH LP AND LP-AT (K080849)Flowcardia, Inc.2008-07-25
CROSSER LP SYSTEM (K080765)Flowcardia, Inc.2008-06-20
MICROSHEATH XL CATHETERS (K073289)Flowcardia, Inc.2008-01-11
THE CROSSER SYSTEM (K072776)Flowcardia, Inc.2007-12-07
THE CROSSER CATHETER, MODEL CR1100 AND SYSTEM ELECTRONICS, MODEL FG1002-02 (K062868)Flowcardia, Inc.2007-01-19
VP SHEATH (K051580)Flowcardia, Inc.2005-10-31
VP WIRE GW140ST (.014 165CM, STANDAR), MODEL GW140ST; VP WIRE GW140SO (.014 165CM, SOFT) MODEL GW140SO (K051062)Flowcardia, Inc.2005-07-15

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