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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