FDA 510(k) Applications Submitted by Karen Provencher

FDA 510(k) Number Submission Date Device Name Applicant
K060309 02/07/2006 AUTOCAT INTRA-AORTIC BALLOON PUMP SERIES ARROW INTL., INC.
K050898 04/11/2005 SMITH & NEPHEW VULCAN ARTICULAR CARTILAGE PROBE, MODEL 721XXXX SMITH & NEPHEW, INC.
K091355 05/08/2009 DEUCE POLYPECTOMY SNARE, MODELS 000995, 000996,000997, 000998 CONMED ENDOSCOPIC TECHNOLOGIES, INC.
K041328 05/19/2004 SMITH & NEPHEW ELECTROBLADE RESECTOR/ADAPTOR SMITH & NEPHEW, INC.
K031675 05/30/2003 SMITH & NEPHEW DYONICS ELECTROBLADE RESECTOR SMITH & NEPHEW, INC.
K041453 06/01/2004 SMITH & NEPHEW TUMESCENT CATHETER INVERSION SYSTEM, MODEL 7210023 SMITH & NEPHEW, INC.
K081580 06/05/2008 BEAMER ARGON SNARE PROBE CONMED CORPORATION
K081644 06/12/2008 BEAMER ARGON PROBE CONMED CORPORATION
K141756 06/30/2014 INFINITY EXPLORER SOFTWARE, C700 FOR IT PATIENT VICINITY WORKSTATION Draeger Medical Systems, Inc.
K172058 07/06/2017 CT6485, CT12885 Analogic Corporation
K032387 08/04/2003 TRIVEX SYSTEM SMITH & NEPHEW, INC.
K182147 08/08/2018 CTXX85 Analogic Corporation
K173569 11/20/2017 Ultrasound System 1300 BK Medical ApS
K034012 12/24/2003 SMITH & NEPHEW RF DENERVATION PROBES & RF CANNULAE SMITH & NEPHEW, INC.


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